FDA Device recall Z-2688-2024
Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/N: 400906-A
- FDA Device
- Class II
- ongoing
- Published 2024-08-28
On 2024-08-28 the FDA classified a Class II recall of Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/N: 400906-A by Intrinsic Therapeutics, citing at least two units have been found to be missing a weld.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2688-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-07-25 |
| Published | 2024-08-28 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Intrinsic Therapeutics |
| Distribution | US |
Product
Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/N: 400906-A
Reason
At least two units have been found to be missing a weld.
Identifiers
| code_info | REF: BAR-IMPACTOR, P/N: 400906-A; UDI-DI: M906IMP1A0; Lot numbers: 10282203, 06152307, 08292301, 10112307. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2688-2024%22
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