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Smith & Nephew, Inc. recalls JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 7-8 , REF 74013988 The JOURNEY II XR Tibial Posterior Keel Punch is a re
Recalled April 3, 2019 · FDA recall Z-1045-2019 · Smith & Nephew
Hazard
Higher than anticipated occurrence of bone fracture during the use of the XR Tibia Posterior Punch · FDA Class II
Units
46 units
Sold at
US Distribution to OR and TN; and Internationally to: Japan.
Description
Higher than anticipated occurrence of bone fracture during the use of the XR Tibia Posterior Punch
Product
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.
Manufacturer(s)
Smith & Nephew, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →