Recall events
/
Event 98907
Event summary
Timeline bucket April 30, 2026
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording Avanos Medical, 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
20 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 20
Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320
Z-2333-2026
Recall number Z-2333-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 231 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2333-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52814]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI 10350770007585, Lot Numbers 30365226 and 30382750
Distribution pattern US Nationwide distribution.
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[335]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 20
Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320
Z-2334-2026
Recall number Z-2334-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 61 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2334-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29338]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI 10350770007554, Lot Numbers 30365227, 30368642, 30374529, 30376099, 30380696, and 30387248
Distribution pattern US Nationwide distribution.
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[226]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 20
Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312
Z-2335-2026
Recall number Z-2335-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 31 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2335-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5934]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information Lot Code: Model No 30-6312, UDI-DI 10350770007547, Lot Number 30365228
Distribution pattern US Nationwide distribution.
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[251]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 20
Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316
Z-2336-2026
Recall number Z-2336-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 41 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2336-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52818]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information Lot Code: Model No 30-6316, UDI-DI 10350770007561, Lot Numbers 30365229 and 30376100
Distribution pattern US Nationwide distribution.
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[257]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 20
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320
Z-2337-2026
Recall number Z-2337-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 49 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2337-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52815]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI 10350770007578, Lot Numbers 30365230, 30367013, 30373825
Distribution pattern US Nationwide distribution.
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[228]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 20
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320
Z-2338-2026
Recall number Z-2338-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 72 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2338-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[46786]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI 10350770007516, Lot Numbers 30365231, 30371022, 30373824, 30378385, 30383807, 30385321
Distribution pattern US Nationwide distribution.
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[219]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 20
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312
Z-2339-2026
Recall number Z-2339-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 43 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2339-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52909]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI 10350770007523, Lot Numbers 30365232, 30367019, 30380107
Distribution pattern US Nationwide distribution.
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[210]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 20
Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-6316 Product Description: Feeding Tube Kit Component: No
Z-2340-2026
Recall number Z-2340-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 54 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2340-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5882]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI 10350770007530, Lot Numbers 30365233, 30367015, 30372821, 30378386
Distribution pattern US Nationwide distribution.
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[340]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 20
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Product Description: Feeding Tube Kit
Z-2341-2026
Recall number Z-2341-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 22 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2341-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29328]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI 10350770007752, Lot Number 30370713
Distribution pattern US Nationwide distribution.
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[255]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2342-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 901 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2342-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[46784]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information Lot Code: Model No 7170-20, UDI-DI 10350770007776, Lot Numbers 30370714, 30373419, 30374048, 30378746
Distribution pattern US Nationwide distribution.
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[264]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2343-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 132 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2343-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52914]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI: 10350770007790, Lot Numbers 30370715, 30371329, 30375466
Distribution pattern US Nationwide distribution.
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[200]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2344-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 208 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2344-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5931]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI 10350770007769, Lot Numbers 30371312 and 30373421
Distribution pattern US Nationwide distribution.
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[267]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2345-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 3,184 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2345-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52813]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI 10350770007783, Lot Numbers 30371313, 30371314, 30373295, 30373296, 30374832, 30378735, 80403340
Distribution pattern US Nationwide distribution.
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[281]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2346-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 1,006 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2346-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52811]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI 10350770007806, Lot Numbers 30371316, 30377829, 80403341
Distribution pattern US Nationwide distribution.
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[263]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2347-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 53 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2347-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[46791]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI 10350770007813, Lot Number 30370718
Distribution pattern US Nationwide distribution.
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[258]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2348-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 1,615 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2348-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29332]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI 10350770007820, Lot Numbers 30371324, 30374833, 30384889, 80403350
Distribution pattern US Nationwide distribution.
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[39092]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2349-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 234 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2349-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5880]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI 10350770007837, Lot Numbers 30371847, 30374834, 30378748, 30380347
Distribution pattern US Nationwide distribution.
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[39096]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2350-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 218 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2350-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[17681]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
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Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI 10350770007844, Lot Numbers 30371318, 30375469, 30383056
Distribution pattern US Nationwide distribution.
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[290]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2351-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 6,005 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2351-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52816]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information Lot Code: Model No 8180-20, UDI-DI 10350770007851, Lot Numbers 20133232, 30371326, 30378749, 30378751, 30379686, 30383063, 30383057, 80403339, 80403342
Distribution pattern US Nationwide distribution.
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[302]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-2352-2026
Initiated April 30, 2026
Classification Class II
Status Ongoing
Quantity 1,205 kits
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Material/Component Contamination
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2352-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[46787]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Code information UDI-DI 10350770007868, Lot Numbers 30371319, 30374055, 30383058, 30386936
Distribution pattern US Nationwide distribution.
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[275]
FDA event record
· Exact recall-number query on openFDA
