Device recall
Z-0836-2013: Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin…
FDA device recall · Class III · Animas Corporation
Key facts
| Recall number (Z-number) | Z-0836-2013 |
|---|---|
| Recall event | 64307 |
| Product | Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin Infusion Pumps Indicated for continuous subcutaneous infusion of insulin. |
| Product code | LZG |
| Recalling firm | Animas Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 24, 2013 |
| 510(k) numbers | K032257, K042873 |
| 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