Device recall
Z-0137-2015: Animas Vibe Insulin Infusion Pump and System. These products are indicated for…
FDA device recall · Class II · Animas Corporation
Key facts
| Recall number (Z-number) | Z-0137-2015 |
|---|---|
| Recall event | 69296 |
| Product | Animas Vibe Insulin Infusion Pump and System. These products are indicated for continuous subcutaneous infusion of insulin for the treatment of insulin-requiring diabetes. |
| Product code | LZG |
| Recalling firm | Animas Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 29, 2015 |
| FEI number | 3002920072 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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