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Cayenne Medical Recalls
3 recalls on record · July 18, 2018 to August 8, 2018 · Medical Devices
August 8, 2018Medical DevicesFDA
Cayenne Medical Inc. recalls Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a. Quattro Spade Drill, for 2.9mm, Model Number CM-93
Hazard: A review of complaints identified a trend for drills breaking.
August 1, 2018Medical DevicesFDA
Cayenne Medical Inc. recalls AperFix Femoral Implant Coring Removal Drill, labeled as the following: a. Femoral Removal Coring Reamer 9mm, Model
Hazard: 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.
July 18, 2018Medical DevicesFDA
Cayenne Medical Inc. recalls AperFix AM Femoral Implant, Model numbers CM-2409 (9mm x 24 mm) and CM-2410 (10 mm x 24 mm). For orthopedic use in liga
Hazard: Potential for AperFix 24 mm implant breaking inside the drilled femoral socket.