MicroPort Orthopedics Inc. 2024-12-25 Health serious FDA
Health · FDA · Recall #FDA-Z-0699-2025
EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; … Recall
Issued December 25, 2024 · MicroPort Orthopedics Inc.
In December 2024, MicroPort Orthopedics Inc. recalled the EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; …, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; … right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact MicroPort Orthopedics Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- MicroPort Orthopedics Inc.
- Category
- Health
- Recall date
- December 25, 2024
- Units affected
- Not reported
- Sold at
- OUS: CN, GR, ES, ZA, FR, JP, IT
- Recall number
- FDA-Z-0699-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- MicroPort Orthopedics Inc. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.