Home / Recalls / Medical Devices
Peter Lazic Gmbh recalls D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.
Recalled March 20, 2024 · FDA recall Z-1279-2024 · Peter Lazic
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. · FDA Class II
Units
10 units
Sold at
US Nationwide distribution in the state of ME.
Description
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, 230mm bayonet, jaw rigid, double action.
Manufacturer(s)
Peter Lazic Gmbh
Made in
Germany
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →