Recall events
/
Event 82865
Event summary
Timeline bucket April 23, 2019
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Arrow International Inc
Dossier provenance
Source snapshots represented here
openFDA Device Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall
event_date_initiated coverage
June 01, 1997–June 30, 2026
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Complete imported group
Every recalled product in this event
36 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
device · product 1 of 36
Arrow PICC powered by Arrow VPS Stylet Product Code: ASK45041JHVA
Z-1787-2019
Recall number Z-1787-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 66 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1787-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[3228]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F17C0310
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28893]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 36
Arrow¿ PICC Kit Product Code: ASK 45541 LVH1
Z-1788-2019
Recall number Z-1788-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 105 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1788-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[45743]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F18E0221
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28598]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 36
Arrow PICC Kit Product Code: ASK 45541 RWJ4
Z-1789-2019
Recall number Z-1789-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 100 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1789-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27038]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code:13F18A0202
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28800]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 36
Arrow PICC Kit pre loaded with Arrow¿ VPS Precision Stylet Product Code: ASK 45552 CRM
Z-1790-2019
Recall number Z-1790-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 190 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1790-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[51181]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code:13F17J0016, 13F17M0213
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28300]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 36
Arrow PICC Kit Product Code: ASK 45552 RWJ4
Z-1791-2019
Recall number Z-1791-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 1840 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1791-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[51204]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code:13F17A0217,13F17D0222, 13F17F0784,13F17G0413, 13F17J0173, 13F18A0118, 13F18G0195, 13R16H0080, 13R17D0222, 13R17G0413
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28711]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 36
Arrow PICC with Chlorag+ard Technology Product Code: CDA 44052 HPK1A
Z-1792-2019
Recall number Z-1792-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 180 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1792-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[22405]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code:23F17J0017,23F17L0593
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28639]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 36
Arrow PICC with Chlorag+ard Technology Product Code: CDA 45041 HPK1A
Z-1793-2019
Recall number Z-1793-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 108 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1793-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[16147]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code:23F17J0249, 23F18E0349
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28581]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 36
Arrow PICC with Chlorag+ard Technology Product Code: CDA 45052 HPK1A
Z-1794-2019
Recall number Z-1794-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 185 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1794-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27028]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code:23F17D0458, 23F17H0763
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28179]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 36
Arrow PICC with Chlorag+ard Technology Product Code: CDA 45541 HPK1A
Z-1795-2019
Recall number Z-1795-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 20 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1795-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[16153]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F17B0665
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28895]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1796-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 159 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1796-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[45725]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F17F0469, 23F17H0682, 23F17L0203
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28995]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1797-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 78 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1797-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[3226]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F17J0053, 23F18C0024
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28691]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1798-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 77 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1798-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[45729]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F17K0694, 23F18K0108
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[29002]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1799-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 96 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1799-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57044]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F18F0716
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28288]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1800-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 84 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1800-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[3227]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F18E0046, 23F18J0269
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28654]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1801-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 174 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1801-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[16152]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F17C0488
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28470]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1802-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 6 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1802-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57042]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F18J0277
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28862]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1803-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 191 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1803-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57047]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F17E0686, 23F18H0290
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28805]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1804-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 12 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1804-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[22402]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F18A0636
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28589]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1805-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 135 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1805-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[51177]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F18B0189
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28817]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1806-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 162 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1806-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57043]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F18H0497
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28275]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1807-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 48 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1807-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57040]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F18L0161
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28715]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1808-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1808-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[45727]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F17K0228
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28206]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1809-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 350 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1809-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[45724]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code :23F17B0463, 23F18E0251
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28873]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1810-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 279 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1810-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27031]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code:23F18A0307, 23F18K0604
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28200]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1811-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 450 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1811-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[16150]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 23F17K0359, 23F18C0027, 23R17K0359
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28906]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1812-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 2 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1812-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[51179]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 13F17F0097
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28624]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1813-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 9 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1813-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27040]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 13F17C0327,13R17C0327
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28673]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1814-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 1 unit
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1814-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[3225]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 13F17F0098
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28308]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1815-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 3 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1815-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[3230]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 13F17F0099
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28991]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1816-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 16 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1816-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[45744]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 13F17F0100
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28305]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1817-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 52 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1817-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[39060]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 13F18H0239
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28517]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1818-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 430 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1818-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[16148]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code:13F17L0170
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28703]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1819-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 983 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1819-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[22404]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code:13F17A0165, 13F17D0327, 13F18A0208, 13F18B0457, 13F18F0416
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28898]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1820-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 991 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1820-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[39068]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code:13F17C0188, 13F18G0948, 13R17C0188
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28659]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1821-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 578 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1821-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57046]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 13F17E0017, 13F17F0523, 13R17F0523
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[28655]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1822-2019
Initiated April 23, 2019
Classification Class II
Status Terminated
Quantity 4345 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidstock states the incorrect expiration date for the product
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1822-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[10977]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidstock states the incorrect expiration date for the product
Code information Batch Code: 13F17B0178, 13F17C0469, 13F17E0120, 13F17G0412,13F17H0393, 13F18A0194
Distribution pattern Nationwide Foreign:
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[29024]
FDA event record
· Exact recall-number query on openFDA
