Device recall
Z-0993-2013: Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is indicated…
FDA device recall · Class I · Animas Corporation
Key facts
| Recall number (Z-number) | Z-0993-2013 |
|---|---|
| Recall event | 64370 |
| Product | Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is indicated for continuous subcutaneous infusion of insulin for the treatment of insulin-requiring diabetes. |
| Product code | LZG |
| Recalling firm | Animas Corporation |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 14, 2015 |
| 510(k) numbers | 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