# FDA recall Z-1052-2023

> **NuVasive Inc** · Class III · device recall initiated 2022-07-19.

## Product

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

## 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.

## Distribution

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

## Key facts

- **Recall number:** Z-1052-2023
- **Recalling firm:** NuVasive Inc
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-07-19
- **Report date:** 2023-02-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Diego, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1052-2023

## Citation

> AI Analytics. FDA recall Z-1052-2023. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1052-2023. Source: US FDA. Licensed CC0.

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