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

Recall Z-2047-2023 — LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left

U.S. FDA — Device Enforcement · Germany · 2021-03-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2047-2023
Date of alert
2021-03-18
Country / jurisdiction
Germany
Risk level
Class II
Risk type
recall
Brand
Waldemar Link GmbH & Co. KG (Mfg Site)
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04026575340736
Reported risk: The firm discovered through customer complaints that device segments may not meet specifications.
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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