Device recall
Z-0161-2016: Nipro Safe Touch TULIP Safety Fistula Needle, FT+152530TP, for use as a blood…
FDA device recall · Class II · Nipro Medical Corporation
Key facts
| Recall number (Z-number) | Z-0161-2016 |
|---|---|
| Recall event | 72365 |
| Product | Nipro Safe Touch TULIP Safety Fistula Needle, FT+152530TP, for use as a blood access device for blood purification and for other treatments requiring an extracorporeal circuit of larger volumes of blood. |
| Product code | LLB |
| Recalling firm | Nipro Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 13, 2017 |
| 510(k) numbers | K071145 |
| 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