Device recall
Z-1668-2013: Medtronic MiniMed Paradigm Insulin Infusion Sets The Paradigm infusion sets are…
FDA device recall · Class I · Medtronic MiniMed
Key facts
| Recall number (Z-number) | Z-1668-2013 |
|---|---|
| Recall event | 65430 |
| Product | Medtronic MiniMed Paradigm Insulin Infusion Sets The Paradigm infusion sets are intended for use with Paradigm insulin infusion pumps. |
| Product code | FPA |
| Recalling firm | Medtronic MiniMed |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 10, 2015 |
| 510(k) numbers | K011071 |
| FEI number | 3003166194 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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