Recall events
/
Event 87915
Event summary
Timeline bucket April 29, 2021
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Medtronic Perfusion Systems
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
25 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 25
Medtronic HY10Z48R2, Ctr., Custom Pack HY10Z48R2 Adult ECC 1/4, Custom Perfusion System, Sterile, Rx.
Z-1871-2021
Recall number Z-1871-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 6 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1871-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[51958]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000292034, Lot #220866332, Use By 2022-09-29
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14560]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 25
Medtronic HY8M63R4, Custom Pack HY8M63R4 Adult ECC, Custom Perfusion System, Sterile, Rx.
Z-1872-2021
Recall number Z-1872-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 2 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1872-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[58295]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00643169921948, Lot #221058527, Use By 2022-10-30
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14325]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 25
Medtronic BB10R94R6, Custom Pack BB10R94R6 1/4 ECCPK, Custom Perfusion System, Sterile, Rx.
Z-1873-2021
Recall number Z-1873-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 10 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1873-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[4861]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000258016, Lot numbers 221102356, Use By 2022-10-09; and 221672011, Use By 2022-10-22
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14493]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 25
Medtronic BB11J14R2, Custom Pack BB11J14R2 Bridge, Custom Perfusion System, Sterile, Rx.
Z-1874-2021
Recall number Z-1874-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 15 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1874-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[51956]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 20763000446516, Lot numbers 22128923, Use By 2022-10-31; and Lot 221815851, Use By 2023-01-18
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14379]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 25
Medtronic HY7M07R6, Custom Pack HY7M07R6 E 1/4, Custom Perfusion System, Sterile, Rx.
Z-1875-2021
Recall number Z-1875-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 27 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1875-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[33502]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00643169981102, Lot numbers 220866430, Use By 2022-04-03; 221102361, Use By 2202-04-03; and 221727287, Use By 2022-09-29.
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14500]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 25
Medtronic CB7J97R8, Custom Pack CB7J97R8 U14 E Sup, Custom Perfusion System, Sterile, Rx.
Z-1876-2021
Recall number Z-1876-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 10 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1876-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[9316]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00643169641228, Lot numbers 220866440, Use By 2022-07-10; and 221451579, Use By 2022-10-24
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14584]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 25
Medtronic HY11B40R1, Custom Pack HY11B40R1 1/4 Respirato, Custom Perfusion System, Sterile, Rx.
Z-1877-2021
Recall number Z-1877-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 18 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1877-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[40103]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000314231, Lot numbers 220911913, Use By 2022-03-13; and 221249923, Use By 2022-10-01
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14598]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 25
Medtronic CB1H18R20, Custom Pack CB1H18R20 Accesory, Custom Perfusion System, Sterile, Rx.
Z-1878-2021
Recall number Z-1878-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 4 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1878-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[28241]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000108328, Lot number 220776249, Use By 2022-07-06
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14504]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 25
Medtronic CB10W63R1, Custom Pack CB10W63R1 HL 20 1/4, Custom Perfusion System, Sterile, Rx.
Z-1879-2021
Recall number Z-1879-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 15 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1879-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[28240]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000341039, Lot number 221196140, Use By 2022-09-24
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14367]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1880-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 12 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1880-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[33500]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000235147, Lot number 221196141, Use By 2022-08-19
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14901]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1881-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 61 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1881-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[9317]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000286378, Lot number 221238939, Use By 2022-03-03
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14316]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1882-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 12 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1882-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[9315]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000341015, Lot numbers 221102372, Use By 2022-09-21; and 221672013, Use By 2022-11-02
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14645]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1883-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 14 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1883-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[9319]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000467449, Lot number 221227814, Use By 2022-08-28
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14895]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1884-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 1 tubing pack
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1884-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[4857]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000341022, Lot number 221332879, Use By 2022-10-05
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14655]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1885-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 11 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1885-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[15574]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000306717, Lot number 221387881, Use By 2022-10-21
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14785]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1886-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 8 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1886-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[28239]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000082987, Lot number 221451509, Use By 2022-10-28.
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14687]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1887-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 16 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1887-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[4858]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000360436, Lot number 221451543, Use By 2022-10-22
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14374]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1888-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 5 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1888-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[51961]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000360443, Lot number 221542968, Use By 2022-11-06
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14898]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1889-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 3 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1889-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[4856]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00643169640870, Lot number 221575680, Use By 2022-11-20
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14651]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1890-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 5 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1890-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[40101]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000156879, Lot number 221679870, Use By 2022-12-03
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14890]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1891-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 25 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1891-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[51962]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000499105, Lot numbers 221719701, Use By 2023-01-06; and 221764442, Use By 2023-01-13
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14486]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1892-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 2 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1892-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[28238]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000458133, Lot number 221249911, Use By 2022-10-22
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14490]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1893-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 26 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1893-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[58294]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00643169984820, Lot 221148857, Use By 2022-10-12
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14320]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1894-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 6 tubing packs
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1894-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[28237]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00763000387044, Lot number 221238931, Use By 2022-10-17
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14591]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1895-2021
Initiated April 29, 2021
Classification Class II
Status Terminated
Quantity 7 tubing sets
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Specific lots may have been manufactured with insufficient or incomplete welds.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Nonconforming Material/Component
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1895-2021
Source locator 0001-device-recall-0001-of-0001.json.zip#results[51960]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Specific lots may have been manufactured with insufficient or incomplete welds.
Code information GTIN 00643169947436, Lot number 221387901, Use By 2022-12-16
Distribution pattern US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military 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[14383]
FDA event record
· Exact recall-number query on openFDA
