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MicroPort Orthopedics Inc. FDA Recalls
6 recalls on file across devices, 0 of them Class I and 3 still open. This firm is not matched to a listed company.
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Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.
| Product |
|---|
| Brand Name: MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE Model/Catalog Number: HTHT0036 Software VersClass IIDec 19, 2025Due to products not having FDA Premarket authorization to be |
| EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEMORAL COMPONENT CS/CRClass IIOct 29, 2024Femoral implant porous size 5 right primary and femoral impl |
| EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are for cemented use onlyClass IIMay 3, 2024One confirmed incident has been received that EFSRN4PR, lot |
| EVOLUTION MP Tibial Bases, Size 2+ LEFT, REF ETPKN2PL, knee tibial baseClass IIOct 28, 2022One confirmed incident has been received that ETPKN2PL lot 1 |
| EVOLUTION MP Tibial Bases, Size 7 LEFT, REF ETPKN7SL, knee tibial baseClass IIOct 28, 2022One confirmed incident has been received that ETPKN2PL lot 1 |
| PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECKClass IIMay 4, 2022One manufacturing lot is missing the plasma-spray coating in |