Class II

Medical Device Recall: D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.

Peter Lazic Gmbh · October 6, 2023

Reason for Recall

Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.

Distribution

US Nationwide distribution in the state of ME.

States Affected

NATIONWIDE

Quantity Affected

63 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1278-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.