Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K190100 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the following reference numbers: ... | 2 | 02/29/2024 |
FEI # 1000395711 United Orthopedic Corporation |
| USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference Numbers: REF: PE25153... | 2 | 02/29/2024 |
FEI # 1000395711 United Orthopedic Corporation |
| USTAR II Knee System Cemented curved stem, RHS, Non Coated for the following reference numbers: R... | 2 | 02/29/2024 |
FEI # 1000395711 United Orthopedic Corporation |
| United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part, RHS, 25 mm Length, Cat... | 2 | 10/14/2021 |
FEI # 3009760038 Uoc Usa Inc |
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