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MicroPort Orthopedics Inc. recalls PROFEMUR(R) MODULAR NECK, HIP FEMORAL NECK MicroPort total hip systems intended for use in total hip arthroplasty for re
Recalled August 24, 2016 · FDA recall Z-2588-2016 · MicroPort Orthopedics
Hazard
Profemur(R) neck, Item Number PHA01222 (Short AR VV2 Ti Neck) was labeled as Item Number PHA01212 (Short AR VV1 Ti Neck). · FDA Class II
Units
14 units
Sold at
Belgium, Italy, Spain, and Poland
Description
Profemur(R) neck, Item Number PHA01222 (Short AR VV2 Ti Neck) was labeled as Item Number PHA01212 (Short AR VV1 Ti Neck).
Product
PROFEMUR(R) MODULAR NECK, HIP FEMORAL NECK MicroPort total hip systems intended for use in total hip arthroplasty for reduction or relief of pain and/or improved hip function in skeletally mature patients.
Manufacturer(s)
MicroPort Orthopedics Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →