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

Recall Z-1045-2019 — JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 7-8 , REF 74013988 The JOURNEY II XR Tibial Posterior Keel Punch is a reusable surgical instrument used to prepare the proximal tibial to receive a JOURNEY II XR tibial baseplate.

U.S. FDA — Device Enforcement · United States · 2018-12-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1045-2019
Date of alert
2018-12-10
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Smith & Nephew, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
74013988
Reported risk: Higher than anticipated occurrence of bone fracture during the use of the XR Tibia Posterior Punch
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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