Reported Jul 10, 2024 · Ongoing
EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are for cemented use only.
MicroPort Orthopedics Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: MicroPort Orthopedics Inc. · 5677 Airline Rd · Arlington, TN · 38002-9501
Is this the product you have?
- EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are for cemented use only.
- Lot codes and dates
- UDIPart
- EFSRN3PLPrimary DI Number M684EFSRN3PL1
- Part EFSRN4PRPrimary DI Number M684EFSRN4PR1
- lot Number's
MP1982097MP1982170
- Catalog Number(s)
EFSRN3PLEFSRN4PR
- Amount recalled
- 40 units
Why it was recalled
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 Evolution MP Non-Porous Femoral Left in the packaging.
This product could cause temporary or reversible health problems — stop using it.
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