NuVasive Inc: Medical Device Recalls in 2020

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by NuVasive Inc in 2020. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

NUVASIVE MAGEC 2 Rod X.X mm XX mm, REF MC2-XXXXS LOT 0000000 AAA - Product Usage: comprised of a sterile single-use spinal rod that is surgically implanted using appropriate NuVasive Reline, Reline Small Stature, and Armada fixation components (i.e. Pedicle screws, hooks and/or connectors, provided non-sterile, to be sterilized by the end user).
Nuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI: 00887517206633 - Product Usage: is intended for intraoperative neurophysiologic monitoring during spinal surgery.