Class II — Peter Lazic Gmbh
| Recalling firm | PETER LAZIC GMBH |
|---|---|
| Registered facility | PETER LAZIC GMBH (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Wrong product coloring. The paddle clips should be blank, but they are colored blue. |
| Product | L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile |
| Quantity | 51 units |
| Distribution | US Nationwide distribution in the state of ME. |
| Initiated | 2023-07-14 |
| Classified | 2024-03-12 |
| Recall number | Z-1288-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Peter Lazic Gmbh (Z-1288-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93952/
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