Device recall
Z-2898-2016: CareLink iPro Version 1.10, Catalog No. MMT-7340 With data obtained from the…
FDA device recall · Class II · Medtronic Inc.
Key facts
| Recall number (Z-number) | Z-2898-2016 |
|---|---|
| Recall event | 74955 |
| Product | CareLink iPro Version 1.10, Catalog No. MMT-7340 With data obtained from the iPro2 recorder and blood glucose meter, the CareLink iPro software retrospectively calibrates sensor data and provides reports of continuous glucose information. CareLink iPro reports show up to seven calendar days of study… |
| Product code | PHV |
| Recalling firm | Medtronic Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 20, 2016 |
| FEI number | 3003166194 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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