Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AperFix AM Femoral Implant Recalled by Cayenne Medical Inc. Due to Potential for AperFix 24 mm implant breaking inside...
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 Cayenne Medical Inc. directly.
Affected Products
AperFix AM Femoral Implant, Model numbers CM-2409 (9mm x 24 mm) and CM-2410 (10 mm x 24 mm). For orthopedic use in ligament reconstruction.
Quantity: 976 units
Why Was This Recalled?
Potential for AperFix 24 mm implant breaking inside the drilled femoral socket.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Cayenne Medical Inc.
Cayenne Medical Inc. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report