Device recall
Z-1052-2023: NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version…
FDA device recall · Class III · NuVasive Inc
Key facts
| Recall number (Z-number) | Z-1052-2023 |
|---|---|
| Recall event | 91294 |
| Product | NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.US |
| Product code | OLO |
| Recalling firm | NuVasive Inc |
| Recall class | Class III |
| Status | Open, Classified |
| 510(k) numbers | K210574 |
| FEI number | 3002980729 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database