NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software… — Class III medical device recall Z-1052-2023
Ongoing recall by NuVasive Inc, reported 2023-02-15, distributed nationwide. Due to an incorrect security key, customers were unable to connect to remote monitoring during spinal surgery,
| Recall number | Z-1052-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | NuVasive Inc, San Diego, CA, United States |
| Recall initiated | 2022-07-19 |
| Classified | 2023-02-03 |
| Reported by FDA | 2023-02-15 |
| Distributed | Nationwide (US) |
| Quantity | 7 |
| Serial numbers | PM00007, PM00017, SM90013, SM90018, SM90021, SM90030, SM90032 |
| Model numbers | 1881500 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1052-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.