NuVasive Recalls
36 recalls on record · November 28, 2012 to February 15, 2023 · Medical Devices
Recalls by year
12
20
22
23
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 15, 2023Medical DevicesFDA
NuVasive Inc recalls NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.US
Hazard: 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 procedures.
December 28, 2022Medical DevicesFDA
NuVasive Inc recalls X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.
Hazard: Potential that insert will be unable to disengage from the vertebral body replacement device/implant
August 3, 2022Medical DevicesFDA
NuVasive Inc recalls Description/Part: Simplify Disc Size 1, Ht 5/SM-5; Simplify Disc Size 1, Ht 6/SM-6; Simplify Disc Size 2, Ht 4/MD-4;
Hazard: Cervical artificial disc Unique Device Identifier (UDI) barcodes contain the incorrect Global Trade Item Number (GTIN) on the Patient Label when scanned and may also contain the incorrect GTIN human readable text, which could lead to selecting an incorrectly sized unit.
July 29, 2020Medical DevicesFDA
NuVasive Inc recalls Nuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI: 00887517206633 - Product Usage: is intended fo
Hazard: 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 correct part number 1747065, NVM5 Harness, Gen 3.5 EM. This issue can result in delay in therapy or lack of EMG neuromonitoring during surgery if the surgeon elects to proceed without the NVM5.
May 13, 2020Medical DevicesFDA
NuVasive Inc recalls NUVASIVE MAGEC 2 Rod X.X mm XX mm, REF MC2-XXXXS LOT 0000000 AAA - Product Usage: comprised of a sterile single-use sp
Hazard: Post-implantation separation of an actuator end cap component that may expose internal components of the actuator, which could lead to hastened degeneration of the internal components and egress of Titanium alloy wear debris and resultant localized tissue discoloration.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 7.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 7.5mm x 45mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 7.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 6.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 6.5mm x 45mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 6.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 5.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 5.5mm x 45mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 5.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 4.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 4.5mm x 35mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls Screw Tulip , 5.5mm Rod Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 7.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 7.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 7.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 7.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 7.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 7.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 6.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 6.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 6.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 6.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 6.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 6.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.
November 28, 2012Medical DevicesFDA
NuVasive Inc recalls 5.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Hazard: The tulip portion of the screw assembly can disengage from the shank after implantation.