Medtronic Neuromodulation recalls

Medtronic Neuromodulation has 86 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 3 Jun 2026. 44 are still ongoing. 4 were reported in the last 12 months.

Total recalls86since 2012

Last 12 months4reported

Class I1315% of total

Ongoing44latest 3 Jun 2026

Recalls per month, last 24 months

click a bar for that month

2Oct '24 1 0 4Jan '25 0 0 2Apr 1 0 0Jul 0 0 0Oct 0 1 1Jan '26 0 0 0Apr 0 2 0Jul 0 0

Severity split

Class I 13 15%Class II 72 84%Class III 1 1%

Why medtronic neuromodulation is recalled

Product types

By year

202633%
202589%
202467%
20231315%
202256%
2021910%
202011%
201911%
201822%
201722%

Ongoing medtronic neuromodulation recalls

44 active

Reported	Class	Recall	Company	Reason	Where
3 Jun 2026Device	CLASS II	Medtronic Pocket Adaptor Kit for Deep Brain Stimulation recalled	Medtronic Neuromodulation	Other	Nationwide
3 Jun 2026Device	CLASS II	Medtronic Pocket Adaptor Kit for Deep Brain Stimulation recalled	Medtronic Neuromodulation	Other	Nationwide
21 Jan 2026Device	CLASS II	A71200 Vanta" Clinician Programmer Application (CP App) recalled	Medtronic Neuromodulation	Device Malfunction	Nationwide
31 Dec 2025Device	CLASS II	Restore Clinician Programmer Application (CP App) recalled	Medtronic Neuromodulation	Device Malfunction	Nationwide
7 May 2025Device	CLASS II	Enhanced Verify Evaluation Handset (CFN HH90130FA) recalled	Medtronic Neuromodulation	Device Malfunction	Nationwide
16 Apr 2025Device	CLASS II	Stimulation RC Clinician Programmer Application recalled	Medtronic Neuromodulation	Device Malfunction	Nationwide

All medtronic neuromodulation recalls, newest first

86 total

Reported	Class	Recall	Company	Reason	Where
3 Jun 2026Device	CLASS II	Medtronic Pocket Adaptor Kit for Deep Brain Stimulation recalled	Medtronic Neuromodulation	Other	Nationwide
3 Jun 2026Device	CLASS II	Medtronic Pocket Adaptor Kit for Deep Brain Stimulation recalled	Medtronic Neuromodulation	Other	Nationwide
21 Jan 2026Device	CLASS II	A71200 Vanta" Clinician Programmer Application (CP App) recalled	Medtronic Neuromodulation	Device Malfunction	Nationwide
31 Dec 2025Device	CLASS II	Restore Clinician Programmer Application (CP App) recalled	Medtronic Neuromodulation	Device Malfunction	Nationwide
7 May 2025Device	CLASS II	Enhanced Verify Evaluation Handset (CFN HH90130FA) recalled	Medtronic Neuromodulation	Device Malfunction	Nationwide
16 Apr 2025Device	CLASS II	Stimulation RC Clinician Programmer Application recalled	Medtronic Neuromodulation	Device Malfunction	Nationwide
9 Apr 2025Device	CLASS II	A820 myPTM recalled by Medtronic Neuromodulation	Medtronic Neuromodulation	Device Malfunction	Nationwide
8 Jan 2025Device	CLASS II	SynchroMed II recalled by Medtronic Neuromodulation	Medtronic Neuromodulation	Device Malfunction	Nationwide
8 Jan 2025Device	CLASS II	SynchroMed II recalled by Medtronic Neuromodulation	Medtronic Neuromodulation	Device Malfunction	Nationwide
8 Jan 2025Device	CLASS II	SynchroMed II recalled by Medtronic Neuromodulation	Medtronic Neuromodulation	Device Malfunction	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.