--- title: "Medtronic Neurosurgery Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Medtronic Neurosurgery 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-neurosurgery/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Medtronic Neurosurgery recall records **10** reported ongoing 10 records in this archive. Latest source date Jun 17, 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 Jun 17, 2026 FDA device enforcement ### [Ventriculostomy Kit, REF: 46154](https://isitonrecall.com/recall/fda-device-z-2768-2026-ventriculostomy-kit-ref-46154/) Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit endotoxin levels that exceed the acceptable limit for devices that come into contact with cerebrospinal fluid; endotoxin exposure can cause... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of UT, AL, CA, NC, GA, AR, LA, KY, LA, KY, IL, OK and the country of Costa Rica. [Official source for Ventriculostomy Kit, REF: 46154](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2768-2026%22) Nov 1, 2024 FDA device enforcement ### [Becker External Drainage and Monitoring System: 24146 EDMS 24146 BECKER NO Y-SITE 25120 EDMS II 25120 BECKER W/1-WAY VALVE 26040 KIT 26040 BECKER EDMS II 27609 BECKER 27609 W/NE...](https://isitonrecall.com/recall/fda-device-z-0661-2025-becker-external-drainage-and-monitoring-system-24146-edms-24146-becker-no-y-site-25120-edms-ii-25120/) Due to complaints received reporting cracks and/or leaks of the stopcocks associated with the external drainage and monitoring system (EDMS). Class I Reported ongoing Distribution: Worldwide distribution. US nationwide including Puerto Rico; Algeria, Argentina, Australia, Austria, Bahrain, Barbados, Bosnia And Herzegovina, Brunei Darussalam, Cambodia, Cana... [Official source for Becker External Drainage and Monitoring System: 24146 EDMS 24146 BECKER NO Y-SITE 25120 EDMS II 2...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0661-2025%22) Nov 1, 2024 FDA device enforcement ### [Exacta External Drainage and Monitoring System: 27581 KIT 27581 EXACTA W/EDM VCATH 35CM 27636 EDM 27636 EXACTA W/BRAIDED CORD LOCK 27666 EDM 27666 EXCTA W GLUE STPCK GR PT LN 27...](https://isitonrecall.com/recall/fda-device-z-0662-2025-exacta-external-drainage-and-monitoring-system-27581-kit-27581-exacta-w-edm-vcath-35cm-27636-edm-276/) Due to complaints received reporting cracks and/or leaks of the stopcocks associated with the external drainage and monitoring system (EDMS). Class I Reported ongoing Distribution: Worldwide distribution. US nationwide including Puerto Rico; Algeria, Argentina, Australia, Austria, Bahrain, Barbados, Bosnia And Herzegovina, Brunei Darussalam, Cambodia, Cana... [Official source for Exacta External Drainage and Monitoring System: 27581 KIT 27581 EXACTA W/EDM VCATH 35CM 27636 EDM...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0662-2025%22) Jan 22, 2024 FDA device enforcement ### [Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, REF 46913, Sterile EO, Rx Only. Used to drain cerebrospinal fluid (CSF) as a means to reduce i...](https://isitonrecall.com/recall/fda-device-z-1162-2024-medtronic-duet-external-drainage-and-monitoring-system-interlink-injection-sites-ref-46913-sterile-e/) Potential for catheter disconnection from the patient line stopcock connectors. Class I Reported ongoing Distribution: Worldwide Distribution: US (nationwide): AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, ... [Official source for Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, REF 46913, Ste...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1162-2024%22) Jan 22, 2024 FDA device enforcement ### [Medtronic Duet External Drainage and Monitoring System, SmartSite, Injection Sites, REF 46914, Sterile EO, Rx Only. Used to drain cerebrospinal fluid (CSF) as a means to reduce ...](https://isitonrecall.com/recall/fda-device-z-1163-2024-medtronic-duet-external-drainage-and-monitoring-system-smartsite-injection-sites-ref-46914-sterile-e/) Potential for catheter disconnection from the patient line stopcock connectors. Class I Reported ongoing Distribution: Worldwide Distribution: US (nationwide): AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, ... [Official source for Medtronic Duet External Drainage and Monitoring System, SmartSite, Injection Sites, REF 46914, St...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1163-2024%22) Jan 22, 2024 FDA device enforcement ### [Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Ventricular Catheter, REF 46915, Sterile EO, Rx Only. Used to drain cerebrospinal fluid (CSF) ...](https://isitonrecall.com/recall/fda-device-z-1164-2024-medtronic-duet-external-drainage-and-monitoring-system-interlink-injection-sites-ventricular-cathete/) Potential for catheter disconnection from the patient line stopcock connectors. Class I Reported ongoing Distribution: Worldwide Distribution: US (nationwide): AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, ... [Official source for Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Ventricular Ca...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1164-2024%22) Jan 22, 2024 FDA device enforcement ### [Medtronic Duet External Drainage and Monitoring System, SmartSite Injection Sites, Ventricular Catheter, REF 46916, Sterile EO, Rx Only. Used to drain cerebrospinal fluid (CSF) ...](https://isitonrecall.com/recall/fda-device-z-1165-2024-medtronic-duet-external-drainage-and-monitoring-system-smartsite-injection-sites-ventricular-cathete/) Potential for catheter disconnection from the patient line stopcock connectors. Class I Reported ongoing Distribution: Worldwide Distribution: US (nationwide): AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, ... [Official source for Medtronic Duet External Drainage and Monitoring System, SmartSite Injection Sites, Ventricular Ca...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1165-2024%22) Jan 22, 2024 FDA device enforcement ### [Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Lumbar Catheter, REF 46917, Sterile EO, Rx Only. Used to drain cerebrospinal fluid (CSF) as a ...](https://isitonrecall.com/recall/fda-device-z-1166-2024-medtronic-duet-external-drainage-and-monitoring-system-interlink-injection-sites-lumbar-catheter-ref/) Potential for catheter disconnection from the patient line stopcock connectors. Class I Reported ongoing Distribution: Worldwide Distribution: US (nationwide): AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, ... [Official source for Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Lumbar Cathete...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1166-2024%22) Jun 28, 2023 FDA device enforcement ### [Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only](https://isitonrecall.com/recall/fda-device-z-2412-2023-medtronic-ref-46915-duet-external-drainage-and-monitoring-system-interlink-injection-sites-ventricul/) Product labeling contains incorrect expiration date Class II Reported ongoing Distribution: US Nationwide distribution in the states of NJ, FL, CA, IL. [Official source for Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Vent...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2412-2023%22) Jun 13, 2023 FDA device enforcement ### [Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; DUREPAIR DURA SUBSTITUTE 3 X 3, 61105; DUREPAIR DURA SUBSTITUTE 1 X 3, 61106; DUREPAIR DURA SUBSTITUTE ...](https://isitonrecall.com/recall/fda-device-z-2207-2023-durepair-dura-regeneration-matrix-durepair-dura-substitute-2-x-2-61100-durepair-dura-substitute-3-x/) Dura regeneration matrix may have out-of-specification endotoxin levels due to issues with in-process and finished goods endotoxin testing, which may present clinically with signs and symptoms of an acute inflammatory process, comparable to infection. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of PR, TX, WA, HI, MI, GA, AL, IL, IN, IA, MO, KY, NY, CA, AZ, PA, UT, ME, MD, MN, FL, AK, NE, VA, OR, WI, NC, LA,... [Official source for Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; DUREPAIR DURA SUBSTITUT...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2207-2023%22) ## Reasons in these listed records - Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit endotoxin levels that exceed the acceptable limit for devices that come into contact with cerebrospinal fluid; endotoxin exposure can cause an acute inflammato... - Due to complaints received reporting cracks and/or leaks of the stopcocks associated with the external drainage and monitoring system (EDMS). - Potential for catheter disconnection from the patient line stopcock connectors. - Product labeling contains incorrect expiration date These examples come from this result page and are not a ranking of every recall reason. ## Checking Medtronic Neurosurgery ### Is there a recall on medtronic neurosurgery right now? This archive contains 10 records, including 10 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 Neurosurgery](https://isitonrecall.com/check/?q=Medtronic%20Neurosurgery) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)