FDA Device recall Z-0923-2022
20/30 Priority Pack w/COPILOT - REF 1003327 WPL2122272-01 (2019-03-01)
- FDA Device
- Class II
- ongoing
- Published 2022-04-20
On 2022-04-20 the FDA classified a Class II recall of 20/30 Priority Pack w/COPILOT - REF 1003327 WPL2122272-01 (2019-03-01) by Abbott Vascular, citing due to an increase in complaint trend for leaks and intermittent/loose connections.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0923-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-03-11 |
| Published | 2022-04-20 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Abbott Vascular |
| Distribution | US |
Product
20/30 Priority Pack w/COPILOT - REF 1003327 WPL2122272-01 (2019-03-01)
Reason
Due to an increase in complaint trend for leaks and intermittent/loose connections.
Identifiers
| code_info | Part Numbers: 1003327 Device Identifier-GTIN: 08717648013973 Lot Numbers: 60308571 60315919 60325098 60308572 6031…Part Numbers: 1003327 Device Identifier-GTIN: 08717648013973 Lot Numbers: 60308571 60315919 60325098 60308572 60316407 60325099 60308573 60317004 60325100 60308574 60317279 60325101 60308575 60317280 60325103 60309671 60317533 60326298 60309672 60317540 60326299 60309673 60317541 60326300 60309674 60317947 60326301 60309675 60317948 60326425 60309676 60318668 60326859 60309677 60318669 60326860 60309681 60318670 60326861 60309682 60319819 60326862 60309683 60320067 60326863 60309684 60320068 60328011 60309685 60320069 60328023 60309686 60320070 60328355 60309687 60320072 60328356 60311341 60320073 60329330 60311342 60320074 60329331 60311343 60320075 60329332 60311344 60320076 60329333 60311345 60320914 60329967 60312167 60322147 60329968 60312168 60322182 60329969 60312169 60322183 60330058 60312170 60322184 60331041 60312171 60322185 60331043 60312172 60323316 60331358 60312173 60323317 60331537 60312174 60323318 60331538 60312175 60323319 60331731 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0923-2022%22
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