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NuVasive Inc recalls NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.US
Recalled February 15, 2023 · FDA recall Z-1052-2023 · NuVasive
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. · FDA Class III
Units
7
Sold at
U.S. Nationwide distribution in the states of CA, FL, NC, OH, and TX.
Description
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.
Product
NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.US
Manufacturer(s)
NuVasive Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →