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

Recall Z-0184-2013 — Knee Components: ROTULE "913" D=32 , Part Number PGA00030, Lot Number X02383380 INSERT TIBIAL "913 PCR" T.1 - EP.10-, PGA00050, Lot Numbers: V11272719, W02300988, W09372781, W09372781, and W10372876 INSERT TIBIAL "913 PCR" T.1 - EP.14-, PGA00054, Lot Number: V0266952 INSERT TIBIAL "913 PCR" T.

U.S. FDA — Device Enforcement · United States · 2012-09-05 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0184-2013
Date of alert
2012-09-05
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Wright Medical Technology Inc
Product category
device
Product type
Devices
Reported risk: There may be inaccuracies on the labeled shelf life on all products packaged at the Toulon, France facility.
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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