Drug recall
CareLink Pro Medtronic CareLink Pro MMT-7335 is a personal computer software application designed to enhance…
FDA recall event 70424 · Class III · Medtronic MiniMed Inc.
Key facts
| Event ID | 70424 |
|---|---|
| Recall numbers | Z-1228-2015 |
| Recalling firm | Medtronic MiniMed Inc. |
| Product type | Devices |
| Products | CareLink Pro Medtronic CareLink Pro MMT-7335 is a personal computer software application designed to enhance Health Care Provider management of diabetic patients using Medtronic insulin pumps and… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The firm is informing customers of a software error that might result in an inaccurate display of the Temp Basal time and duration in CareLink Clinical reports with data uploaded from the MiniMed 620G… |
| Initiation date | Nov 10, 2014 |
| Report date | Mar 11, 2015 |
| Termination date | Mar 10, 2015 |
| City | Northridge |
| State | CA |
| Country | United States |
| FEI number | 3003166194 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: