FDA Device recall Z-0921-2022
20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (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 INDEFLATOR -REF 1000184 WPL2122268-01 (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-0921-2022 |
| 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 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)
Reason
Due to an increase in complaint trend for leaks and intermittent/loose connections.
Identifiers
| code_info | Part Numbers: 1000184 Device Identifier-GTIN: 08717648013591 Lot Numbers: 60309678 60320071 60337162 60311336 6032…Part Numbers: 1000184 Device Identifier-GTIN: 08717648013591 Lot Numbers: 60309678 60320071 60337162 60311336 60320899 60337166 60311338 60331726 60311337 60311339 60331727 60317539 60315914 60334491 60318209 60317535 60334492 |
|---|
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-0921-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.