L-Aneurysm Clip TITANIUM Paddle-Clip — Class II medical device recall Z-1288-2024
Ongoing recall by Peter Lazic Gmbh, reported 2024-03-20, distributed nationwide. Wrong product coloring. The paddle clips should be blank, but they are colored blue.
| Recall number | Z-1288-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Peter Lazic Gmbh, Tuttlingen, N/A, Germany |
| Recall initiated | 2023-07-14 |
| Classified | 2024-03-12 |
| Reported by FDA | 2024-03-20 |
| Distributed | Nationwide (US) |
| Quantity | 51 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 04250603733799 |
| Serial numbers | LW36020, LW36021, LW36022, LW36023, LW36024, LW36025, LW36026, LW36027, LX61385 |
| Model numbers | 45.782 |
Product
L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile
Reason for recall
Wrong product coloring. The paddle clips should be blank, but they are colored blue.
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-1288-2024. 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.