Drug recall
Medtronic Power Supply 26907, Medtronic CareLink Encore(TM) 29901 Programmer
FDA recall event 81950 · Class II · Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Key facts
| Event ID | 81950 |
|---|---|
| Recall numbers | Z-0845-2019 |
| Recalling firm | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Product type | Devices |
| Products | Medtronic Power Supply 26907, Medtronic CareLink Encore(TM) 29901 Programmer |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | There is a potential for an electrical short circuit to develop in a subset of 479 Model 26907 power supply cable plugs that connect to the Medtronic Model 29901 CareLink Encore programmer. A failure… |
| Initiation date | Jan 17, 2019 |
| Report date | Feb 27, 2019 |
| Termination date | Mar 30, 2021 |
| City | Mounds View |
| State | MN |
| Country | United States |
| FEI number | 2182208 |
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: