Device recall
Z-1705-2009: Paradigm Quick-set Infusion Sets, Models MMT-396, MMT-397, MMT-398 and MMT-399…
FDA device recall · Class I · Medtronic MiniMed
Key facts
| Recall number (Z-number) | Z-1705-2009 |
|---|---|
| Recall event | 52521 |
| Product | Paradigm Quick-set Infusion Sets, Models MMT-396, MMT-397, MMT-398 and MMT-399. The Paradigm Quick-set infusion sets are intended for use in combination with Paradigm reservoirs (models MMT- 326 or MMT-332) and Paradigm external insulin infusion pumps to deliver insulin (subcutaneously) to patients… |
| Product code | FPA |
| Recalling firm | Medtronic MiniMed |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Nov 8, 2010 |
| 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