--- title: "Medtronic Neuromodulation Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Medtronic Neuromodulation recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/medtronic-neuromodulation/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Medtronic Neuromodulation recall records **43** reported ongoing 45 records in this archive. Latest source date May 13, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status May 13, 2026 FDA device enforcement ### [Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, implanted, for parkinsonian tremor](https://isitonrecall.com/recall/fda-device-z-2240-2026-medtronic-1x4-pocket-adaptor-kit-for-deep-brain-stimulation-model-64001-stimulator-electrical-implan/) A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and The countries of Austria, France, Germany, Italy, Japan, Latvia, Netherlands, Poland, Spain, Sweden, Switzerland, United Kingdom. [Official source for Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical,...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2240-2026%22) May 13, 2026 FDA device enforcement ### [Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical, implanted, for parkinsonian tremor](https://isitonrecall.com/recall/fda-device-z-2241-2026-medtronic-2x4-pocket-adaptor-kit-for-deep-brain-stimulation-model-64002-stimulator-electrical-implan/) A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and The countries of Austria, France, Germany, Italy, Japan, Latvia, Netherlands, Poland, Spain, Sweden, Switzerland, United Kingdom. [Official source for Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical,...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2241-2026%22) Apr 8, 2026 FDA device enforcement ### [Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on the following devices: 1. PROG CT900A CLINICIAN TABLET US, Model Number CT900...](https://isitonrecall.com/recall/fda-device-z-2201-2026-medtronic-synchromed-flex-infusion-mode-a810-clinician-programmer-software-application-loaded-on-the/) 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 ord... Class II Reported ongoing Distribution: Worldwide distribution. [Official source for Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2201-2026%22) Dec 3, 2025 FDA device enforcement ### [A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on Samsung tablets (CFN CT900).](https://isitonrecall.com/recall/fda-device-z-1043-2026-a71200-vanta-clinician-programmer-application-cp-app-version-2-0-2465-and-2-0-2683-product-number-a7/) Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonged or postponed surgical procedure. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product nu...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1043-2026%22) Nov 20, 2025 FDA device enforcement ### [Restore Clinician Programmer Application (CP App), Model A71100 used with the following programmers: CT900A PROG CT900A CLINICIAN TABLET US CT900B PROG CT900B CLINICIAN TABLET E...](https://isitonrecall.com/recall/fda-device-z-0996-2026-restore-clinician-programmer-application-cp-app-model-a71100-used-with-the-following-programmers-ct9/) 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 surgica... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Argentina, Aruba, Australia, Austria, Belgium, Bosnia And Herzegovina, Brazil, Canada, Canary Islands, Chile, China, ... [Official source for Restore Clinician Programmer Application (CP App), Model A71100 used with the following programme...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0996-2026%22) Apr 3, 2025 FDA device enforcement ### [Enhanced Verify Evaluation Handset (CFN HH90130FA)](https://isitonrecall.com/recall/fda-device-z-1704-2025-enhanced-verify-evaluation-handset-cfn-hh90130fa/) Evaluation handsets may not be able to communicate with the neurostimulator due to handsets having a faster processing speed than prior handsets. An inability to connect may cause the therapy to stop being delivered and a system error will be displayed. Pat... Class II Reported ongoing Distribution: US Nationwide distribution including in the states of AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, LA, MA, MD, MI, MN, MS, NC, NE, NJ, NM, NY, OH, OR, PA, TX, WA, WI. [Official source for Enhanced Verify Evaluation Handset (CFN HH90130FA)](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1704-2025%22) Mar 4, 2025 FDA device enforcement ### [Stimulation RC Clinician Programmer Application, Model A71400, when used with the Inceptiv (Model 977119) and Intellis Pro (Model 977118) neurostimulators](https://isitonrecall.com/recall/fda-device-z-1543-2025-stimulation-rc-clinician-programmer-application-model-a71400-when-used-with-the-inceptiv-model-97711/) There is a software issue that can permanently disable communication with an implantable neurostimulator (INS) when a specific intraoperative programming sequence is used. Class II Reported ongoing Distribution: Worldwide Distribution: US (Nationwide) and OUS (Global) to countries of: Austria, Belgium, Bulgaria, Canary Islands, Cyprus, Croatia, Czech Republic, Denmark, Finland, France, ... [Official source for Stimulation RC Clinician Programmer Application, Model A71400, when used with the Inceptiv (Model...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1543-2025%22) Jan 9, 2025 FDA device enforcement ### [A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.](https://isitonrecall.com/recall/fda-device-z-1506-2025-a820-myptm-software-application-associated-with-medtronic-synchromed-pump-and-infusion-system/) Product complaints were received describing the A820 myPTM app taking longer than expected for patients to interact with their implantable pump. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Belgium, Canary Islands, Czech Republic, France, Germany, Greece, Ireland, Italy, Netherlands, Norway, Portu... [Official source for A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1506-2025%22) Nov 21, 2024 FDA device enforcement ### [SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CLINICIAN TABLET EU -UK with the A810 CP app version 2.x, CFN CT900B](https://isitonrecall.com/recall/fda-device-z-0771-2025-synchromed-ii-model-8637-and-synchromed-iii-model-8667-implantable-pumps-used-with-prog-ct900b-clini/) Software issues were identified in application version 2.x. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CL...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0771-2025%22) Nov 21, 2024 FDA device enforcement ### [SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900C CLINICIAN TABLET UK with the A810 CP app version 2.x, CFN CT900C](https://isitonrecall.com/recall/fda-device-z-0772-2025-synchromed-ii-model-8637-and-synchromed-iii-model-8667-implantable-pumps-used-with-prog-ct900c-clini/) Software issues were identified in application version 2.x. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900C CL...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0772-2025%22) Nov 21, 2024 FDA device enforcement ### [SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CLINICIAN TABLET GLOBAL with the A810 CP app version 2.x, CFN CT900D](https://isitonrecall.com/recall/fda-device-z-0773-2025-synchromed-ii-model-8637-and-synchromed-iii-model-8667-implantable-pumps-used-with-prog-ct900d-clini/) Software issues were identified in application version 2.x. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CL...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0773-2025%22) Nov 21, 2024 FDA device enforcement ### [SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900E CLINICIAN TABLET GLBL SMSNG and PROG CT900E CLINICIAN TABLET PAPER EN with the A81...](https://isitonrecall.com/recall/fda-device-z-0774-2025-synchromed-ii-model-8637-and-synchromed-iii-model-8667-implantable-pumps-used-with-prog-ct900e-clini/) Software issues were identified in application version 2.x. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900E CL...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0774-2025%22) Sep 24, 2024 FDA device enforcement ### [Medtronic Percept RC Implantable Neurostimulators (INS), Model B35300.](https://isitonrecall.com/recall/fda-device-z-0206-2025-medtronic-percept-rc-implantable-neurostimulators-ins-model-b35300/) A limited number of Percept RC Implantable Neurostimulators (INS), Model B35300 will not be able to communicate with the A610 DBS Clinician Programmer Application upon use and an "Invalid Device" message will appear. Class II Reported ongoing Distribution: International distribution to the countries of Germany, UK, and Israel. [Official source for Medtronic Percept RC Implantable Neurostimulators (INS), Model B35300.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0206-2025%22) Sep 18, 2024 FDA device enforcement ### [Medtronic Recharger Kits, RS6230, RS7230, and RS5220A, containing components WR9230 and WR9220A Recharger for rechargeable implantable neurostimulators. The Rechargers are used ...](https://isitonrecall.com/recall/fda-device-z-0372-2025-medtronic-recharger-kits-rs6230-rs7230-and-rs5220a-containing-components-wr9230-and-wr9220a-recharge/) The Wireless Rechargers in the kits may be unable to enter a recharging session upon first use. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AL, AZ, CA, FL, GA, ID, MD, MI, MN, MO, NC, NJ, OH, PA, SC, TX, VA, and WA. The countries of Austria, Belgium, Denmark, F... [Official source for Medtronic Recharger Kits, RS6230, RS7230, and RS5220A, containing components WR9230 and WR9220A R...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0372-2025%22) Sep 11, 2024 FDA device enforcement ### [SynchroMed II Infusion Pump. Product Number: 8637-20](https://isitonrecall.com/recall/fda-device-z-0137-2025-synchromed-ii-infusion-pump-product-number-8637-20/) Potential for error and inability to interrogate pump due to data corruption in the pump memory. Class II Reported ongoing Distribution: US Nationwide distribution in the state of Mississippi. [Official source for SynchroMed II Infusion Pump. Product Number: 8637-20](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0137-2025%22) Aug 21, 2024 FDA device enforcement ### [Vanta Implantable Neurostimulator (INS), Model 977006](https://isitonrecall.com/recall/fda-device-z-0132-2025-vanta-implantable-neurostimulator-ins-model-977006/) Model 977006 Vanta INS batterty life has depleted faster than HCPs or patients expected leading to outpatient reprogramming or earlier than anticipated surgical replacements. Class II Reported ongoing Distribution: Worldwide distribution. [Official source for Vanta Implantable Neurostimulator (INS), Model 977006](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0132-2025%22) Jun 17, 2024 FDA device enforcement ### [Medtronic Handset with Communicator, Model TH90Q01, InterStim Smart Programmer and Communicator Kits, containing the Model HH90 Handset and the TM90 Communicator.](https://isitonrecall.com/recall/fda-device-z-3073-2024-medtronic-handset-with-communicator-model-th90q01-interstim-smart-programmer-and-communicator-kits-c/) A subset of the handsets within the kit may not be able to complete the pairing process with the communicator upon initial setup. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Medtronic Handset with Communicator, Model TH90Q01, InterStim Smart Programmer and Communicator K...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3073-2024%22) May 15, 2024 FDA device enforcement ### [A610 Clinician Programmer (CP) Software Application (app) with the following versions: Version 2.0.x (2.0.4584, 2.0.4594, 2.0.4605, 2.0.4630, and 2.0.4648), Version 3.0.x (3.0.1...](https://isitonrecall.com/recall/fda-device-z-2427-2024-a610-clinician-programmer-cp-software-application-app-with-the-following-versions-version-2-0-x-2-0/) Patients implanted with a pocket adaptor (Model 64001 and/or 64002) are limited to HEAD ONLY MRI eligibility. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Algeria, Argentina, Australia, Austria, Belgium, Bolivia, Brazil, Canada, Canary Islands, China, Colombia, Costa Rica... [Official source for A610 Clinician Programmer (CP) Software Application (app) with the following versions: Version 2....](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2427-2024%22) May 10, 2024 FDA device enforcement ### [Medtronic Ascenda Intrathecal Catheter, Models: a) 8780 (114 cm); b) 8781 (140 cm); c) 8784 (catheter pump revision kit)](https://isitonrecall.com/recall/fda-device-z-2352-2024-medtronic-ascenda-intrathecal-catheter-models-a-8780-114-cm-b-8781-140-cm-c-8784-catheter-pump-revis/) Design update to the Ascenda Intrathecal Catheter Models 8780, 8781, and 8784. The intent of the design update is to reduce the potential for tissue growth into the Ascenda catheter connector which may potentially lead to catheter occlusion. Class II Reported ongoing Distribution: Worldwide Distribution: US (nationwide) and OUS (foreign) countries of: Argentina, Aruba, Australia, Austria, Belgium, Brazil, Canada, Canary Islands, Chile, Colombia, Cyprus, C... [Official source for Medtronic Ascenda Intrathecal Catheter, Models: a) 8780 (114 cm); b) 8781 (140 cm); c) 8784 (cath...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2352-2024%22) Mar 28, 2024 FDA device enforcement ### [Intellis AdaptiveStim Product Number 97715, Spinal Cord Stimulator](https://isitonrecall.com/recall/fda-device-z-1691-2024-intellis-adaptivestim-product-number-97715-spinal-cord-stimulator/) inability to reprogram one device Class II Reported ongoing Distribution: International distribution in the country of UK. [Official source for Intellis AdaptiveStim Product Number 97715, Spinal Cord Stimulator](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1691-2024%22) ## Reasons in these listed records - A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates. - 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, ... - Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonged or postponed surgical procedure. - 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... These examples come from this result page and are not a ranking of every recall reason. ## Checking Medtronic Neuromodulation ### Is there a recall on medtronic neuromodulation right now? This archive contains 45 records, including 43 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Medtronic Neuromodulation](https://isitonrecall.com/check/?q=Medtronic%20Neuromodulation) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)