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

Recall Z-2899-2018 — QUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF TAPPING SCREWS, Part Number 12-01521S The Stryker QuickFlap Sterile Procedure Pack is intended for reconstruction, stabilization and/or rigid fixation of non-load bearing bony areas subsequent to craniotomy, craniectomy and cranial fractures

U.S. FDA — Device Enforcement · Germany · 2018-06-22 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2899-2018
Date of alert
2018-06-22
Country / jurisdiction
Germany
Risk level
Class II
Risk type
recall
Brand
Stryker Leibinger GmbH & Co. KG
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
1000193584
Reported risk: After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
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.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.