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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
Recalled July 18, 2018 · FDA recall Z-2422-2018 · Cayenne Medical
Hazard
Potential for AperFix 24 mm implant breaking inside the drilled femoral socket. · FDA Class II
Units
976 units
Sold at
US nationwide distribution.
Description
Potential for AperFix 24 mm implant breaking inside the drilled femoral socket.
Product
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.
Manufacturer(s)
Cayenne Medical Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →