Peter Lazic Gmbh Recalls
5 recalls from federal safety databases (FDA, CPSC). Sourced directly from government enforcement feeds.
Medical Device Recalls (5)
- Class II
October 6, 2023
D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action.
Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
- Class II
October 6, 2023
D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.
Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
- Class II
October 6, 2023
D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.
Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
- Class II
July 14, 2023
L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile
Wrong product coloring. The paddle clips should be blank, but they are colored blue.
- Class II
July 14, 2023
L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile
Wrong product coloring. The paddle clips should be blank, but they are colored blue.
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