Barricaid Annular Closure Impactor — Class II medical device recall Z-2688-2024
Ongoing recall by Intrinsic Therapeutics, Inc., reported 2024-08-28, distributed nationwide. At least two units have been found to be missing a weld.
| Recall number | Z-2688-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Intrinsic Therapeutics, Inc., Woburn, MA, United States |
| Recall initiated | 2024-07-25 |
| Classified | 2024-08-20 |
| Reported by FDA | 2024-08-28 |
| Distributed | Nationwide (US) |
| Quantity | 207 units |
| Lot numbers | 06152307, 08292301, 10112307, 10282203 |
| Model numbers | 400906-A |
Product
Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/N: 400906-A
Reason for recall
At least two units have been found to be missing a weld.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2688-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.