Device recall
Z-2544-2014: Medtronic MiniMed Paradigm Insulin Infusion Pumps, Paradigm models: MMT-511…
FDA device recall · Class II · Medtronic MiniMed Inc.
Key facts
| Recall number (Z-number) | Z-2544-2014 |
|---|---|
| Recall event | 68277 |
| Product | Medtronic MiniMed Paradigm Insulin Infusion Pumps, Paradigm models: MMT-511, MMT-512, MMT-712, MMT-712E, MMT-515, MMT-715, MMT-522, MMT-522K, MMT-722, MMT-722K, MMT-523, MMT-523K, MMT-723, MMT-723K, MMT-554, and MMT-754. MiniMed 530G: MMT-551, and MMT-751 Paradigm insulin infusion pumps are intended… |
| Product code | OYC |
| Recalling firm | Medtronic MiniMed Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 7, 2015 |
| PMA numbers | P120010, P980022 |
| FEI number | 3003166194 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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