Recall Atlas

MicroPort Orthopedics recalls

5 official recalls and safety alerts involving MicroPort Orthopedics since 2022-06, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with MicroPort Orthopedics or the relevant agency.

  1. 2026-01-28
  2. US
    Drugs & medicalClass II

    MicroPort Orthopedics Inc. recalls Brand Name: MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE Model/Catalog Number: HTHT0036 Software Version: N/A Product…

    Due to products not having FDA Premarket authorization to be distributed within the United States.

    FDA · DeviceMicroPort Orthopedics Inc.The product was sent to distributors in multiple US states, including Texas,…Official notice →
  3. 2024-12-25
  4. US
    Drugs & medicalClass II

    MicroPort Orthopedics Inc. recalls EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEMORAL COMPONENT CS/CR NON-POROUS SIZE…

    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.

    FDA · DeviceMicroPort Orthopedics Inc.OUS: CN, GR, ES, ZA, FR, JP, ITOfficial notice →
  5. 2024-07-10
  6. US
    Drugs & medicalClass II

    MicroPort Orthopedics Inc. recalls EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are for cemented use only.

    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 number MP1982097, Size 3…

    FDA · DeviceMicroPort Orthopedics Inc.International distribution in the country of China. There is no field…Official notice →
  7. 2023-02-22
  8. US
    Drugs & medicalClass II

    MicroPort Orthopedics Inc. recalls EVOLUTION MP Tibial Bases, Size 7 LEFT, REF ETPKN7SL, knee tibial base

    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 Base, in the packaging.

    FDA · DeviceMicroPort Orthopedics Inc.International Distribution to countries of: Germany, Italy, France, Belgium,…Official notice →
  9. 2022-06-08
  10. US
    Drugs & medicalClass II

    MicroPort Orthopedics Inc. recalls PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK

    One manufacturing lot is missing the plasma-spray coating in the proximal region of the stem body.

    FDA · DeviceMicroPort Orthopedics Inc.Worldwide distribution - US Nationwide distribution in the states of FL, IN,…Official notice →