Device recall
Z-0288-2021: Instructions For Use document of the GPS Trackers.
FDA device recall · Class II · Blue Ortho
Key facts
| Recall number (Z-number) | Z-0288-2021 |
|---|---|
| Recall event | 86491 |
| Product | Instructions For Use document of the GPS Trackers. |
| Product code | OLO |
| Recalling firm | Blue Ortho |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 31, 2023 |
| 510(k) numbers | K193618 |
| FEI number | 3008027912 |
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