Medical DeviceJan 28, 2026
MicroPort HIPTURN FEM HEAD TRIAL 36MM REUSABLE recall — FDA Z-1133-2026
Due to products not having FDA Premarket authorization to be distributed within the United States.
Class IIFDA: OngoingMicroPort Orthopedics Inc.
Recall history in this database
Classification mix: Class II: 7, Class I: 2.
Medical DeviceDec 25, 2024
MicroPort Orthopedics EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF recall — FDA Z-0699-2025
Femoral implant porous size 5 right primary and femoral implant non-porous size 6 left primary have correct markings on devices, but may have incorrect packaging.
Class IIFDA: OngoingMicroPort Orthopedics Inc.
Medical DeviceJul 10, 2024
MicroPort Orthopedics EVOLUTION MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee recall — FDA Z-2244-2024
One confirmed incident has been received that EFSRN4PR, lot number MP1982170, Size 4 Evolution MP Non-Porous Femoral Right was opened during surgery and contained part number EFSRN3PL, lot…
Class IIFDA: OngoingMicroPort Orthopedics Inc.
Medical DeviceFeb 22, 2023
MicroPort Orthopedics EVOLUTION MP Tibial Bases, Size 7 LEFT, REF ETPKN7SL, knee tibial base recall — FDA Z-0276-2023
One confirmed incident has been received that ETPKN2PL lot 1916559, size 2 Evolution MP Tibial Base, was opened during surgery and contained ETPKN7SL lot 1916715, size 7 Evolution MP Tibial…
Class IIFDA: OngoingMicroPort Orthopedics Inc.
Medical DeviceFeb 22, 2023
MicroPort Orthopedics EVOLUTION MP Tibial Bases, Size 2+ LEFT, REF ETPKN2PL, knee tibial recall — FDA Z-0275-2023
One confirmed incident has been received that ETPKN2PL lot 1916559, size 2 Evolution MP Tibial Base, was opened during surgery and contained ETPKN7SL lot 1916715, size 7 Evolution MP Tibial…
Class IIFDA: OngoingMicroPort Orthopedics Inc.
Medical DeviceJun 8, 2022
MicroPort Orthopedics PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK recall — FDA Z-1225-2022
One manufacturing lot is missing the plasma-spray coating in the proximal region of the stem body.
Class IIFDA: TerminatedMicroPort Orthopedics Inc.
Medical DeviceSep 30, 2020
MicroPort Orthopedics PROFEMUR Neck Long Titanium, Catalog Numbers: PHA01204, PHA01214 recall — FDA Z-2941-2020
MicroPort Orthopedics Inc. states that there have been reports of fractures of the long and extra-long Titanium modular femoral neck component after implantation. Worldwide there were 680…
Class IFDA: TerminatedMicroPort Orthopedics Inc.
Medical DeviceSep 30, 2020
MicroPort Orthopedics PROFEMUR Neck Extra Long Titanium, Catalog Numbers: PHA01206 recall — FDA Z-2942-2020
MicroPort Orthopedics Inc. states that there have been reports of fractures of the long and extra-long Titanium modular femoral neck component after implantation. Worldwide there were 680…
Class IFDA: TerminatedMicroPort Orthopedics Inc.
Medical DeviceSep 16, 2020
MicroPort Orthopedics PROFEMUR Titanium and Cobalt Chrome modular necks, Item Numbers and recall — FDA Z-2948-2020
MicroPort Orthopedics Inc. is voluntarily recalling any existing inventory of PROFEMUR Titanium and Cobalt Chrome modular necks with previous package insert versions to replace the PROFEMUR…
Class IIFDA: OngoingMicroPort Orthopedics Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies MicroPort Orthopedics Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.