Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AperFix Femoral Implant Coring Removal Drill Recalled by Cayenne Medical Inc. Due to A review of product complaints in 2010 identified...
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 Femoral Implant Coring Removal Drill, labeled as the following: a. Femoral Removal Coring Reamer 9mm, Model Number CM-7109; b. Femoral Removal Coring Reamer 10mm, Model Number CM-7110; c. Femoral Removal Coring Reamer 11mm, Model Number CM-7111; d. Femoral Removal Coring Reamer 9 mm - Long, Model Number CM-7129; e. Femoral Removal Coring Reamer 10 mm - Long, Model Number CM-7130; f. Femoral Removal Coring Reamer 11 mm - Long, Model Number CM-7131; Orthopedic surgical instrument.
Quantity: 1,444 units total
Why Was This Recalled?
A review of product complaints in 2010 identified a trend for the Coring Removal Drill of premature wear and/or breakage. This recall occurred in 2013.
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