Drug recall
Restore Clinician Programmer Application (CP App), Model A71100 used with the following programmers: CT900A…
FDA recall event 98028 · Class II · Medtronic Neuromodulation
Key facts
| Event ID | 98028 |
|---|---|
| Recall numbers | Z-0996-2026 |
| Recalling firm | Medtronic Neuromodulation |
| Product type | Devices |
| Products | Restore Clinician Programmer Application (CP App), Model A71100 used with the following programmers: CT900A PROG CT900A CLINICIAN TABLET US CT900B PROG CT900B CLINICIAN TABLET EU -UK CT900C PROG… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Software issue where a Device Reset message displayed on the app was unable to be cleared. In rare cases, this resulted in an inability to resume therapy, and the patient experienced a recurrence of… |
| Initiation date | Nov 20, 2025 |
| Report date | Dec 31, 2025 |
| 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: