fda
23 records
FDA Device Recall: NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version
2023-02-15
Class III — Due to an incorrect security key, customers were unable to connect to remote monitoring during spinal surgery, neck dissections, thoracic surgeries, and upper and lower extremity procedure...
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FDA Device Recall: Nuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI: 008875
2020-07-29
Class II — The NVM5 EMG Module kit intended for intraoperative neurophysiologic monitoring during spinal surgery contains incorrect component, part number 1715945, SSEP harness instead of the the corr...
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FDA Recall: NuVasive Inc — Class II
20121128
The tulip portion of the screw assembly can disengage from the shank after implantation. | Product: 6.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
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FDA Recall: NuVasive Inc — Class II
20121128
The tulip portion of the screw assembly can disengage from the shank after implantation. | Product: 7.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
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FDA Recall: NuVasive Inc — Class II
20121128
The tulip portion of the screw assembly can disengage from the shank after implantation. | Product: 7.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
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FDA Device Recall: 6.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 7.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 7.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 5.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 6.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 6.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: Screw Tulip , 6.25mm Rod Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 7.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 6.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 7.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 6.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 6.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 6.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 7.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 5.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 5.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 4.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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FDA Device Recall: 5.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
2012-11-28
Class II — The tulip portion of the screw assembly can disengage from the shank after implantation.
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ny_corps
1 records
NY Corp: NUVASIVE, LLC
2025-07-16
FOREIGN LIMITED LIABILITY COMPANY | County: Albany | Jurisdiction: Delaware
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