FDAOctober 6, 2023device
D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
What to do
FDA enforcement status: Ongoing
Brands named
peter lazicpeter
UPCs
04250603739593
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAD-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.2023-10-06
- FDAD-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.2023-10-06
- FDAL-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile2023-07-14
- FDAL-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile2023-07-14
- CPSCWedgwood Decorative Baby Rattles Recalled by WWRD Due to Choking Hazard2016-02-04
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