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 | Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip. |
| Product | D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action. |
| Quantity | 26 units |
| Distribution | US Nationwide distribution in the state of ME. |
| Initiated | 2023-10-06 |
| Classified | 2024-03-11 |
| Recall number | Z-1277-2024 |
| 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-1277-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93938/
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