Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GENESIS(R) II CRUCIATE RETAINING ARTICULAR INSERT Recalled by Smith & Nephew Inc Due to The products were produced using the wrong color...
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
GENESIS(R) II CRUCIATE RETAINING ARTICULAR INSERT, TRIAL, SIZE 3-4, A/P 48 MM, M/L 68 MM, QTY 1, NON-STERILE, REF 71430490, Product Usage: Orthopedic
Quantity: 9 units
Why Was This Recalled?
The products were produced using the wrong color material, resulting in the devices being red (used for deep dished inserts) instead of blue (used for cruciate retaining inserts).
Where Was This Sold?
International only: Germany, France, United Arab Emirates, and United Kingdom.
About Smith & Nephew Inc
Smith & Nephew Inc has 26 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report