FDA Device recall Z-1278-2024
D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action
- FDA Device
- Class II
- ongoing
- Published 2024-03-20
On 2024-03-20 the FDA classified a Class II recall of D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action by Peter Lazic, citing customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1278-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-10-06 |
| Published | 2024-03-20 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Peter Lazic |
| Distribution | US |
Product
D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.
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.
Identifiers
| code_info | Model number: 35.411; UDI/DI: 04250603739609; All Lot numbers. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1278-2024%22
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