Class II
Medical Device Recall: D-Clip Standard/Mini Applier, 190mm 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
26 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1277-2024
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.