Device recall
Z-0408-03: The following brand name labeled products are under recall (all catalog numbers…
FDA device recall · Class II · Nipro Corp
Key facts
| Recall number (Z-number) | Z-0408-03 |
|---|---|
| Recall event | 25052 |
| Product | The following brand name labeled products are under recall (all catalog numbers and all lot numbers under recall): NIPRO SafeTouch Safety Fistula Needle, Baxter Safety AV Fistula Set and EXEL Secure Touch Safety AV Fistula Needle Set. |
| Product code | FIE |
| Recalling firm | Nipro Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 15, 2008 |
| 510(k) numbers | K002813 |
| FEI number | 1000132332 |
At a glance
- 1–9 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