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

Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 16mm Stem Base, REF 200252903, Size 3 — recall Z-0139-2023

U.S. FDA — Device Enforcement · United States · 2022-09-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0139-2023
Date of alert
2022-09-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Wright Medical Technology, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00840420124142
Reported risk: The tibial tray lock detail is oversized (larger than specification).
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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