NuVasive Inc FDA Recalls

3 recalls on file across devices, 0 of them Class I and 3 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.Class IINov 10, 2022Potential that insert will be unable to disengage from the v	Potential that insert will be unable to disengage from the vertebral body replacement device/implant	Class IIDevices	Nov 10, 2022
NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.USClass IIIJul 19, 2022Due to an incorrect security key, customers were unable to c	Due to an incorrect security key, customers were unable to connect to remote monitoring during spinal surgery,	Class IIIDevices	Jul 19, 2022
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;Class IIJun 20, 2022Cervical artificial disc Unique Device Identifier (UDI) barc	Cervical artificial disc Unique Device Identifier (UDI) barcodes contain the incorrect Global Trade Item Numbe	Class IIDevices	Jun 20, 2022