Official recall record
Restore Clinician Programmer Application (CP App), Model A71100 used with the following programmers: CT900A PROG CT900A CLINICIAN TABLET
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2025-11-20
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00763000273668
- Brand on record
- Medtronic Neuromodulation
What the authority reported
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 underlying pain symptoms. Resolution would require surgical replacement of the INS.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Same barcode in other registries
The same EAN appears in 1 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.
- 2020-07-17 · US FDA — Medical Devices
Restore Clinician Programmer Application Software, model number A71100, used with the Restore Neurostimulators.
Other recalls from this brand
- 2026-04-08 · US FDA — Medical Devices
Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on the follow - 2025-04-03 · US FDA — Medical Devices
Enhanced Verify Evaluation Handset (CFN HH90130FA)
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