Device recall
Z-1876-2018: Nipro Blood Tubing set with Priming Set and Transducer Protectors. Each device…
FDA device recall · Class II · Nipro Medical Corporation
Key facts
| Recall number (Z-number) | Z-1876-2018 |
|---|---|
| Recall event | 79834 |
| Product | Nipro Blood Tubing set with Priming Set and Transducer Protectors. Each device is packaged in a film pouch with 24 lines per case. The Nipro Set - Blood Tubing Set with Transducer Protector and Priming Set are disposable bloodlines intended to provide extracorporeal access to the patient s blood… |
| Product code | FJK |
| Recalling firm | Nipro Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 19, 2021 |
| 510(k) numbers | K072024 |
| FEI number | 1000132332 |
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