Device recall
Z-0990-2014: Orbit soft Infusion sets, 9 mm soft cannula, P10 (42") tubing; Single-Use Set…
FDA device recall · Class II · Perrigo Diabetes Care
Key facts
| Recall number (Z-number) | Z-0990-2014 |
|---|---|
| Recall event | 67154 |
| Product | Orbit soft Infusion sets, 9 mm soft cannula, P10 (42") tubing; Single-Use Set Orbit Infusion Sets are sterile, non-pyrogenic, single-use devices intended to be used for subcutaneous delivery of medication , for example insulin, from an external infusion pump. |
| Product code | FKB |
| Recalling firm | Perrigo Diabetes Care |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 5, 2014 |
| FEI number | 1811666 |
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