Peter Lazic Gmbh FDA Recalls

5 recalls on file across devices, 0 of them Class I and 5 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.Class IIOct 6, 2023Customer complaint received that reported the applier failed	Customer complaint received that reported the applier failed during surgery. The applier did not release the c	Class IIDevices	Oct 6, 2023
D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.Class IIOct 6, 2023Customer complaint received that reported the applier failed	Customer complaint received that reported the applier failed during surgery. The applier did not release the c	Class IIDevices	Oct 6, 2023
D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action.Class IIOct 6, 2023Customer complaint received that reported the applier failed	Customer complaint received that reported the applier failed during surgery. The applier did not release the c	Class IIDevices	Oct 6, 2023
L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, SterileClass IIJul 14, 2023Wrong product coloring. The paddle clips should be blank, bu	Wrong product coloring. The paddle clips should be blank, but they are colored blue.	Class IIDevices	Jul 14, 2023
L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-SterileClass IIJul 14, 2023Wrong product coloring. The paddle clips should be blank, bu	Wrong product coloring. The paddle clips should be blank, but they are colored blue.	Class IIDevices	Jul 14, 2023