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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
Related Medical Device Recalls
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Product Description
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Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-2117-2023 - Medtronic Catalyft LS Expandable Interbody System, Anterier Standalone Cage, REF 981023322, spinal implant 2 07/10/2023 Medtronic Sofamor Danek USA Inc
Z-2118-2023 - Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981023325, spinal implant 2 07/10/2023 Medtronic Sofamor Danek USA Inc
Z-2119-2023 - Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981025522, spinal implant 2 07/10/2023 Medtronic Sofamor Danek USA Inc
Z-2123-2023 - Medtronic Catalyft LS Expandable Interbody System Implant Kit, Anterior Standalone Cage, REF SPS03188, spinal implant kit 2 07/10/2023 Medtronic Sofamor Danek USA Inc
Z-2121-2023 - Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981027722, spinal implant 2 07/10/2023 Medtronic Sofamor Danek USA Inc
Z-2122-2023 - Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981027725, spinal implant 2 07/10/2023 Medtronic Sofamor Danek USA Inc
Z-2120-2023 - Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981025525, spinal implant 2 07/10/2023 Medtronic Sofamor Danek USA Inc
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