Device recall
Z-1501-2016: CareLink iPro2 Reports, Model No. MMT-7340 is software intended to…
FDA device recall · Class II · Medtronic MiniMed Inc.
Key facts
| Recall number (Z-number) | Z-1501-2016 |
|---|---|
| Recall event | 73451 |
| Product | CareLink iPro2 Reports, Model No. MMT-7340 is software intended to retrospectively calibrates sensor data and provides reports of continuous glucose information |
| Product code | OUG |
| Recalling firm | Medtronic MiniMed Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 16, 2016 |
| 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