Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Apex Knee System. Model Numbers: KC-50090 Recalled by CORIN MEDICAL, LTD. Due to Investigation has identified that the age of the...
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 CORIN MEDICAL, LTD. directly.
Affected Products
Apex Knee System. Model Numbers: KC-50090, KC-50097, KC-50110, KC-50117, KC-50130, KC-50135, KC-50137, KC-50150, KC-50155, KC-50157, KC-50170, KC-50175, KC-50177, KC-50190, KC-50197, KC-52104, KC-52554, KC-52574, KC-52774, KC-55223, KC-55243
Quantity: 341 units
Why Was This Recalled?
Investigation has identified that the age of the nylon packaging material has caused a loss of integrity of some pouches.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About CORIN MEDICAL, LTD.
CORIN MEDICAL, LTD. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report