Drug recall
Clinician Programmer Application (CPA) model A610 Clinician Software Application
FDA recall event 88761 · Class II · Medtronic Neuromodulation
Key facts
| Event ID | 88761 |
|---|---|
| Recall numbers | Z-0201-2022 |
| Recalling firm | Medtronic Neuromodulation |
| Product type | Devices |
| Products | Clinician Programmer Application (CPA) model A610 Clinician Software Application |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | A software anomaly may occur with the clinician programmer application. |
| Initiation date | Sep 23, 2021 |
| Report date | Nov 10, 2021 |
| City | Minneapolis |
| State | MN |
| Country | United States |
| FEI number | 2182207 |
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: