Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 5-6 Recalled by Smith & Nephew, Inc. Due to Higher than anticipated occurrence of bone fracture during...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Smith & Nephew, Inc. directly.
Affected Products
JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 5-6 , 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.
Quantity: 65 units
Why Was This Recalled?
Higher than anticipated occurrence of bone fracture during the use of the XR Tibia Posterior Punch
Where Was This Sold?
This product was distributed to 2 states: OR, TN
About Smith & Nephew, Inc.
Smith & Nephew, Inc. has 220 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report