Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1278-2024 — D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.

U.S. FDA — Device Enforcement · Germany · 2023-10-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1278-2024
Date of alert
2023-10-06
Country / jurisdiction
Germany
Risk level
Class II
Risk type
recall
Brand
Peter Lazic Gmbh
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04250603739609
Reported risk: Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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