Device recall
Z-0624-03: NEEDLEZAP, a battery operated needle destruction device. The product is labeled…
FDA device recall · Class II · E Med Future Inc
Key facts
| Recall number (Z-number) | Z-0624-03 |
|---|---|
| Recall event | 25039 |
| Product | NEEDLEZAP, a battery operated needle destruction device. The product is labeled and marketed for use only in the law enforcement market or veterinary market. |
| Product code | MTV |
| Recalling firm | E Med Future Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 5, 2004 |
| FEI number | 3003763354 |
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