Medtronic Neuromodulation recalls
5 recalls filed under Medtronic Neuromodulation. The most recent was published June 3, 2026.
-
Class II · 5 months ago
Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002 recall: A limited number of Pocket Adaptor Kits, Model 64001 and 64002
A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.
-
Class II · 5 months ago
Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001 recall: A limited number of Pocket Adaptor Kits, Model 64001 and 64002
A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.
-
Class II · 5 months ago
Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer recall: Software issue: When programming the SynchroMed Pump with the A810 CP App
Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged…
-
Class II · 9 months ago
Medtronic Neuromodulation A71200 Vanta" Clinician Programmer Application version recall: Complaints received that Vanta A71200 CP App does not function as intended
Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonged or postponed surgical…
-
Class II · 10 months ago
Medtronic Neuromodulation Restore Clinician Programmer Application recall: Software issue where a Device Reset message displayed on the app was unable
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…
About this page
Medtronic Neuromodulation appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.