Device recall
Z-1898-2020: NUVASIVE MAGEC 2 Rod X.X mm XX mm, REF MC2-XXXXS LOT 0000000 AAA - Product…
FDA device recall · Class II · NuVasive Inc
Key facts
| Recall number (Z-number) | Z-1898-2020 |
|---|---|
| Recall event | 85495 |
| Product | NUVASIVE MAGEC 2 Rod X.X mm XX mm, REF MC2-XXXXS LOT 0000000 AAA - Product Usage: comprised of a sterile single-use spinal rod that is surgically implanted using appropriate NuVasive Reline, Reline Small Stature, and Armada fixation components (i.e. Pedicle screws, hooks and/or connectors, provided… |
| Product code | PGN |
| Recalling firm | NuVasive Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 25, 2022 |
| 510(k) numbers | K171791 |
| FEI number | 3002980729 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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