NuVasive Inc: Medical Device Recall in 2023 - (Recall #: Z-1052-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.US

Product Classification:

Class III

Date Initiated: July 19, 2022

Date Posted: February 15, 2023

Recall Number: Z-1052-2023

Event ID: 91294

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 7

Code Information:

Part Number: 1881500 UDI Code: 0887517PLS137YJ Serial Numbers: PM00017 SM90018 SM90013 SM90021 PM00007 SM90032 SM90030

Distribution Pattern:

U.S. Nationwide distribution in the states of CA, FL, NC, OH, and TX.

Voluntary or Mandated:

Voluntary: Firm initiated