FDADecember 10, 2018device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Higher than anticipated occurrence of bone fracture during the use of the XR Tibia Posterior Punch

What to do

FDA enforcement status: Terminated

Brands named

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Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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