Device recall
Z-1575-2014: NavioPFSTM System, Orthopedic Sterotaxic Instrument, model #'s NPFS-02000…
FDA device recall · Class II · Blue Belt Technologies MN
Key facts
| Recall number (Z-number) | Z-1575-2014 |
|---|---|
| Recall event | 68015 |
| Product | NavioPFSTM System, Orthopedic Sterotaxic Instrument, model #'s NPFS-02000, NPFS-02010, NPFS 02020. |
| Product code | OLO |
| Recalling firm | Blue Belt Technologies MN |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 10, 2014 |
| 510(k) numbers | K121936 |
| FEI number | 3010266064 |
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