Device recall
Z-0307-06: Isulin Pump. Model IR1000
FDA device recall · Class II · Animas Corporation
Key facts
| Recall number (Z-number) | Z-0307-06 |
|---|---|
| Recall event | 33950 |
| Product | Isulin Pump. Model IR1000 |
| Product code | LZG |
| Recalling firm | Animas Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 23, 2005 |
| 510(k) numbers | K021439 |
| FEI number | 3002920072 |
At a glance
- 1–9 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