Medtronic Neuromodulation Recalls

3 recalls found for Medtronic Neuromodulation. Check if any of your products are affected.

HIGH
FDA DEVICE

Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on the following devices: 1. PROG CT900A CLINICIAN TABLET US, Model Number CT900A; 2. PROG...

Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive order, from earliest to latest. However, in rare cases, the steps may be displayed out of order. If this occurs, the programmed Flex Infusion schedule will not be delivered at the intended time, if at all.

Medtronic Neuromodulation
Software issue:
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medtronic Recalls Vanta Clinician Programmer Software Over Functionality Issues

Medtronic Neuromodulation recalled 7,123 units of the Vanta Clinician Programmer Application on December 3, 2025. The software may not function as intended, potentially delaying surgical procedures. Healthcare providers and patients must stop using the software immediately.

Medtronic Neuromodulation
Complaints received
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medtronic Recalls Clinician Programmer App Over High-Risk Software Issue

Medtronic Neuromodulation recalled 7,667 Clinician Programmer Applications on November 20, 2025. A software issue may prevent patients from resuming therapy, leading to a recurrence of pain symptoms. Affected models include A71100 and associated tablets.

Medtronic Neuromodulation
Software issue
Read more

Brand Statistics

Total Recalls
3
Pages
1

Related Brands

GLYCOPYRROLATEZimmer SurgicalEthicon Endo-SurgeryStuffed FoodsStryker Sustainability SolutionsBlue WaveAisstxoerMeridian Bioscience