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. 43 are still ongoing. 4 were reported in the last 12 months.

Total recalls86since 2012

Last 12 months4reported

Class I1315% of total

Ongoing43latest 3 Jun 2026

Recalls per month, last 24 months

click a bar for that month

1Nov '24 0 4 0Feb 0 2 1May 0 0 0Aug 0 0 0Nov 1 1 0Feb 0 0 0May 2 0 0Aug 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

43 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
8 Jan 2025Device	CLASS II	SynchroMed II recalled by Medtronic Neuromodulation	Medtronic Neuromodulation	Device Malfunction	Nationwide
20 Nov 2024Device	CLASS II	Medtronic Recharger Kits, RS6230, RS7230, and RS5220A recalled	Medtronic Neuromodulation	Other	Nationwide
30 Oct 2024Device	CLASS II	Medtronic Percept RC Implantable Neurostimulators (INS) recalled	Medtronic Neuromodulation	Other	MN
30 Oct 2024Device	CLASS II	SynchroMed II Infusion Pump recalled by Medtronic Neuromodulation	Medtronic Neuromodulation	Other	Nationwide
18 Sep 2024Device	CLASS II	Medtronic Handset with Communicator recalled	Medtronic Neuromodulation	Device Malfunction	Nationwide
8 May 2024Device	CLASS II	Intellis AdaptiveStim Product Number 97715, Spinal Cord Stimulator recalled	Medtronic Neuromodulation	Other	MN
31 Jan 2024Device	CLASS II	Model A710 Intellis Clinician Programmer Application, version recalled	Medtronic Neuromodulation	Other	MN
29 Nov 2023Device	CLASS II	Model 97745 Controller used with Models 97715 and 97716 Intellis recalled	Medtronic Neuromodulation	Other	MN
8 Nov 2023Device	CLASS II	Lead 3387s-40 Stimloc Dbs recalled by Medtronic Neuromodulation	Medtronic Neuromodulation	Packaging Defects	4 states
25 Oct 2023Device	CLASS II	SenSight Connector Plug recalled by Medtronic Neuromodulation	Medtronic Neuromodulation	Other	Nationwide
11 Oct 2023Device	CLASS II	Restore Clinician Programmer Application recalled	Medtronic Neuromodulation	Device Malfunction	Nationwide
16 Aug 2023Device	CLASS II	Medtronic InterStim Ground Pad recalled by Medtronic Neuromodulation	Medtronic Neuromodulation	Other	MN
2 Aug 2023Device	CLASS II	A901 Communication Manager Application, used recalled	Medtronic Neuromodulation	Device Malfunction	MN
5 Jul 2023Device	CLASS II	Vanta with AdaptiveStim Implantable Neurostimulator recalled	Medtronic Neuromodulation	Other	MN
26 Apr 2023Device	CLASS II	Medtronic SenSight Extension Tunneler Kit recalled	Medtronic Neuromodulation	Other	Nationwide
18 Jan 2023Device	CLASS II	Vanta/Seqenita LT Clinician Programmer Application recalled	Medtronic Neuromodulation	Device Malfunction	MN
18 Jan 2023Device	CLASS II	Vanta/Seqenita LT Clinician Programmer Application recalled	Medtronic Neuromodulation	Device Malfunction	MN
18 Jan 2023Device	CLASS II	Vanta/Seqenita LT Clinician Programmer Application recalled	Medtronic Neuromodulation	Device Malfunction	MN
18 Jan 2023Device	CLASS II	Vanta/Seqenita LT Clinician Programmer Application recalled	Medtronic Neuromodulation	Device Malfunction	MN
18 Jan 2023Device	CLASS II	Vanta/Seqenita LT Clinician Programmer Application recalled	Medtronic Neuromodulation	Device Malfunction	MN

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.