Device recall
Z-0202-2012: Medtronic MiniMed paradigm mio Infusion Sets MMT-921 The Paradigm mio infusion…
FDA device recall · Class II · Medtronic Minimed
Key facts
| Recall number (Z-number) | Z-0202-2012 |
|---|---|
| Recall event | 59960 |
| Product | Medtronic MiniMed paradigm mio Infusion Sets MMT-921 The Paradigm mio infusion sets are intended for the subcutaneous infusion of insulin from a Medtronic MiniMed Paradigm insulin infusion pum. |
| Product code | FPA |
| Recalling firm | Medtronic Minimed |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 14, 2011 |
| 510(k) numbers | K051264 |
| 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