Device recall
Z-1608-2014: Ultrasound needles, 22G (0.7 mm) x 50mm, packaged individually, 10 needles/box…
FDA device recall · Class II · RM Temena GmbH
Key facts
| Recall number (Z-number) | Z-1608-2014 |
|---|---|
| Recall event | 68026 |
| Product | Ultrasound needles, 22G (0.7 mm) x 50mm, packaged individually, 10 needles/box, item number REF USC050-22. Needles for peripheral nerve blocking under ultrasound guidance. |
| Product code | BSP |
| Recalling firm | RM Temena GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 19, 2016 |
| 510(k) numbers | K080603 |
| FEI number | 3005379387 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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