Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
JOURNEY II UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM Recalled by Smith & Nephew, Inc. Due to A mispack occurred during the manufacturing process, resulting...
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 UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM
Quantity: 12 units
Why Was This Recalled?
A mispack occurred during the manufacturing process, resulting in the box incorrectly containing JOURNEY II UNI Tibia Insert Medical Size 1-2 12MM instead of the JOURNEY II UNI Tibia Insert Medial Size 7-8 8MM.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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