D-Clip Standard/Mini Applier — Class II medical device recall Z-1277-2024
Ongoing recall by Peter Lazic Gmbh, reported 2024-03-20, distributed nationwide. Customer complaint received that reported the applier failed during surgery. The applier did not release the c
| Recall number | Z-1277-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Peter Lazic Gmbh, Tuttlingen, N/A, Germany |
| Recall initiated | 2023-10-06 |
| Classified | 2024-03-11 |
| Reported by FDA | 2024-03-20 |
| Distributed | Nationwide (US) |
| Quantity | 26 units |
| UPC / GTIN / UDI-DI | 04250603739593 |
| Model numbers | 35.410 |
Product
D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action.
Reason for recall
Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
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-1277-2024. 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.