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U.S. Department of Health and Human Services

Medical Device Recalls

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41 to 48 of 48 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-1547-2023 - LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 11 MM X 50 MM Item Number: 15-2230/07 2 05/04/2023 Linkbio Corp.
Z-1548-2023 - LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 13 MM X 50 MM Item Number: 15-2230/08 2 05/04/2023 Linkbio Corp.
Z-1549-2023 - LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 9 MM X 55 MM Item Number: 15-2230/10 2 05/04/2023 Linkbio Corp.
Z-1550-2023 - LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 11 MM X 55 MM Item Number: 15-2230/11 2 05/04/2023 Linkbio Corp.
Z-1551-2023 - LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 13 MM X 55 MM Item Number: 15-2230/12 2 05/04/2023 Linkbio Corp.
Z-1552-2023 - LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 8 MM X 45 MM Item Number: 15-2230/13 2 05/04/2023 Linkbio Corp.
Z-1553-2023 - LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 8 MM X 50 MM Item Number: 15-2230/14 2 05/04/2023 Linkbio Corp.
Z-1508-2023 - LINK SLED Knee System: ENDO SLED KNEE FEM COMP, MEDIUM SMALL Item Number: 15-2020/46 2 05/04/2023 Linkbio Corp.
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