FDA Device recall Z-0924-2022
INDEFLATOR Plus 30 - REF 1000183 WPL2122277-01 (2019-03-01)
- FDA Device
- Class II
- ongoing
- Published 2022-04-20
On 2022-04-20 the FDA classified a Class II recall of INDEFLATOR Plus 30 - REF 1000183 WPL2122277-01 (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-0924-2022 |
| 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
INDEFLATOR Plus 30 - REF 1000183 WPL2122277-01 (2019-03-01)
Reason
Due to an increase in complaint trend for leaks and intermittent/loose connections.
Identifiers
| code_info | Part Numbers: 1000183 Device Identifier-GTIN: 08717648013584 Lot Numbers: 60316775 60322179 60328352 60322176 60326322 60337153 |
|---|
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-0924-2022%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.