Device recall
Z-0570-04: Template Needle, Series 17, 20 cm, with Threaded Female hub and Bent Stylet…
FDA device recall · Class II · Alpha-Omega Services Inc
Key facts
| Recall number (Z-number) | Z-0570-04 |
|---|---|
| Recall event | 27709 |
| Product | Template Needle, Series 17, 20 cm, with Threaded Female hub and Bent Stylet, Closed-End, Disposable. Packaged in single, 10, 15, 20 per package. |
| Product code | MIJ |
| Recalling firm | Alpha-Omega Services Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 29, 2004 |
| FEI number | 2022694 |
At a glance
- None 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