--- title: "Boston Scientific Corporation Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Boston Scientific Corporation recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/boston-scientific-corporation/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Boston Scientific Corporation recall records **352** reported ongoing 354 records in this archive. Latest source date Aug 6, 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 Aug 6, 2026 FDA device enforcement ### [LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS US, Model Number 7260, All Versions (Current 7.8)](https://isitonrecall.com/recall/fda-device-z-3081-2026-lux-dx-lux-dx-ii-lux-dx-ii-insertable-cardiac-monitor-system-server-sw-lat-clarity-ds-us-model-numbe/) There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification of an AF Burden Alert may delay clinical evaluation or therapeutic intervention of an at... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS US, Mod...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3081-2026%22) Aug 6, 2026 FDA device enforcement ### [LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS EU, Model Number 7246, All Versions (Current 7.7)](https://isitonrecall.com/recall/fda-device-z-3082-2026-lux-dx-lux-dx-ii-lux-dx-ii-insertable-cardiac-monitor-system-server-sw-lat-clarity-ds-eu-model-numbe/) There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification of an AF Burden Alert may delay clinical evaluation or therapeutic intervention of an at... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS EU, Mod...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3082-2026%22) Aug 6, 2026 FDA device enforcement ### [LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS ANZ, Model Number 7248, All Versions (Current 7.7)](https://isitonrecall.com/recall/fda-device-z-3083-2026-lux-dx-lux-dx-ii-lux-dx-ii-insertable-cardiac-monitor-system-server-sw-lat-clarity-ds-anz-model-numb/) There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification of an AF Burden Alert may delay clinical evaluation or therapeutic intervention of an at... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS ANZ, Mo...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3083-2026%22) Jul 22, 2026 FDA device enforcement ### [Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1) DVI to HDMI Cable, (1) DisplayPort Cable REF: M0067933000...](https://isitonrecall.com/recall/fda-device-z-3188-2026-boston-scientific-corporation-stonesmart-connect-console-contents-1-power-cord-1-power-adaptor-1-dvi/) A subset of power adapters used with the connect console may exhibit higher-than-expected resistance in the electrical grounding path. As a result, the power adaptor may fail electrical safety testing during installation. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of AZ, FL, CA, OR, IL, NC, NE, UT, CO, OH, AR, NM, AL, WI, TN, IN, GA, OH, WI, KY, CT, KS, SC, IL, NE, MO, MS, DE,... [Official source for Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adap...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3188-2026%22) Jul 14, 2026 FDA device enforcement ### [OverStitch Suture Cinch, 1pk. Endoscopic tissue approximation device.](https://isitonrecall.com/recall/fda-device-z-2961-2026-overstitch-suture-cinch-1pk-endoscopic-tissue-approximation-device/) Device may fail to deploy the cinch implant and/or fail to cut the suture as intended. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Azerbaijan, Belgium, Bulgaria, Canada, Chile, Costa Rica, Croatia, Czech Republic, Denmark, Dominican Republ... [Official source for OverStitch Suture Cinch, 1pk. Endoscopic tissue approximation device.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2961-2026%22) Jul 14, 2026 FDA device enforcement ### [Suture Cinch Long 1pk. Endoscopic tissue approximation device.](https://isitonrecall.com/recall/fda-device-z-2962-2026-suture-cinch-long-1pk-endoscopic-tissue-approximation-device/) Device may fail to deploy the cinch implant and/or fail to cut the suture as intended. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Azerbaijan, Belgium, Bulgaria, Canada, Chile, Costa Rica, Croatia, Czech Republic, Denmark, Dominican Republ... [Official source for Suture Cinch Long 1pk. Endoscopic tissue approximation device.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2962-2026%22) Jul 9, 2026 FDA device enforcement ### [Boston Scientific ENROUTE Transcarotid Neuroprotection System, Material Number SR-200-NPS; Percutaneous catheter](https://isitonrecall.com/recall/fda-device-z-2977-2026-boston-scientific-enroute-transcarotid-neuroprotection-system-material-number-sr-200-nps-percutaneou/) Potential for arterial sheath tip separation or partial tip separation during use. Class I Reported ongoing Distribution: Worldwide distribution: US (nationwide) and OUS (foreign) to countries of: Australia, Canada, China, Jamaica [Official source for Boston Scientific ENROUTE Transcarotid Neuroprotection System, Material Number SR-200-NPS; Percut...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2977-2026%22) Jul 9, 2026 FDA device enforcement ### [Boston Scientific ENROUTE Transcarotid Neuroprotection System Plus, Material Number SR-250-NPS; Percutaneous catheter](https://isitonrecall.com/recall/fda-device-z-2978-2026-boston-scientific-enroute-transcarotid-neuroprotection-system-plus-material-number-sr-250-nps-percut/) Potential for arterial sheath tip separation or partial tip separation during use. Class I Reported ongoing Distribution: Worldwide distribution: US (nationwide) and OUS (foreign) to countries of: Australia, Canada, China, Jamaica [Official source for Boston Scientific ENROUTE Transcarotid Neuroprotection System Plus, Material Number SR-250-NPS; P...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2978-2026%22) Jun 30, 2026 FDA device enforcement ### [Rapid Refill Continuous Injection System, UPN M00566001](https://isitonrecall.com/recall/fda-device-z-2725-2026-rapid-refill-continuous-injection-system-upn-m00566001/) Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe loosening or disconnecting from the manifold, resulting in loose connection or complete disconnection. May lead to difficulty connecting sy... Class II Reported ongoing Distribution: US Nationwide distribution. OUS consignee list pending. [Official source for Rapid Refill Continuous Injection System, UPN M00566001](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2725-2026%22) Jun 30, 2026 FDA device enforcement ### [Radial Jaw 4 Standard Capacity Biopsy Forceps with the following descriptions and UPN: 1. Radial Jaw 4 SC 240cm Box 20; Outer Box UPN: M00513401; Inner Box UPN: M00513400. 2. Ra...](https://isitonrecall.com/recall/fda-device-z-2838-2026-radial-jaw-4-standard-capacity-biopsy-forceps-with-the-following-descriptions-and-upn-1-radial-jaw-4/) Potential for breach in sterile barrier of device packaging. Class II Reported ongoing Distribution: US Nationwide distribution including in the states of AL, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KY, MA, MD, ME, MN, MO, MS, MT, NC, NJ, NM, NY, OH, PA, PR, SC, TN, TX, UT, VA, VT,... [Official source for Radial Jaw 4 Standard Capacity Biopsy Forceps with the following descriptions and UPN: 1. Radial ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2838-2026%22) Jun 30, 2026 FDA device enforcement ### [Radial Jaw 4 Large Capacity Biopsy Forceps with the following descriptions and UPN: 1. Radial Jaw 4 LC 240cm Box 20; Outer Box UPN: M00513321; Inner Box UPN: M00513320. 2. Radia...](https://isitonrecall.com/recall/fda-device-z-2839-2026-radial-jaw-4-large-capacity-biopsy-forceps-with-the-following-descriptions-and-upn-1-radial-jaw-4-lc/) Potential for breach in sterile barrier of device packaging. Class II Reported ongoing Distribution: US Nationwide distribution including in the states of AL, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KY, MA, MD, ME, MN, MO, MS, MT, NC, NJ, NM, NY, OH, PA, PR, SC, TN, TX, UT, VA, VT,... [Official source for Radial Jaw 4 Large Capacity Biopsy Forceps with the following descriptions and UPN: 1. Radial Jaw...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2839-2026%22) Jun 30, 2026 FDA device enforcement ### [Radial Jaw 4 Jumbo Biopsy Forceps with the following descriptions and UPN: Radial Jaw 4 Jumbo 240cm Box 5; Outer Box UPN: M00513363; Inner Box UPN: M00513360.](https://isitonrecall.com/recall/fda-device-z-2840-2026-radial-jaw-4-jumbo-biopsy-forceps-with-the-following-descriptions-and-upn-radial-jaw-4-jumbo-240cm-b/) Potential for breach in sterile barrier of device packaging. Class II Reported ongoing Distribution: US Nationwide distribution including in the states of AL, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KY, MA, MD, ME, MN, MO, MS, MT, NC, NJ, NM, NY, OH, PA, PR, SC, TN, TX, UT, VA, VT,... [Official source for Radial Jaw 4 Jumbo Biopsy Forceps with the following descriptions and UPN: Radial Jaw 4 Jumbo 240...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2840-2026%22) Jun 19, 2026 FDA device enforcement ### [Boston Scientific TheraSphere 360 Y-90 Management Platform, Model Number M00139509001; Radiological Image Processing System.](https://isitonrecall.com/recall/fda-device-z-2771-2026-boston-scientific-therasphere-360-y-90-management-platform-model-number-m00139509001-radiological-im/) Software anomaly occurs when a user adds one or more vials to the cart and subsequently returns to the Activity Calculator to modify one or more input. When a user modifies an input and selects "Recalculate", the dose calculation is updated correctly; howev... Class II Reported ongoing Distribution: US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, FL, GA, IL, IN, LA, MA, MN, NE, NY, OH, OK, OR, SC, SD, TN, TX, UT, WA, WI, WV, WY. [Official source for Boston Scientific TheraSphere 360 Y-90 Management Platform, Model Number M00139509001; Radiologic...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2771-2026%22) Jun 11, 2026 FDA device enforcement ### [FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401; Percutaneous Cardiac Ablation Catheter](https://isitonrecall.com/recall/fda-device-z-2750-2026-farastar-ablation-generator-eu-pulsed-field-ablation-generator-product-id-61m401-percutaneous-cardia/) Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information. Class II Reported ongoing Distribution: International distribution in the states of Austria, Spain, France, Germany, Denmark, Italy, Portugal, Great Britain, Ireland. [Official source for FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401; Percutaneous ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2750-2026%22) Jun 11, 2026 FDA device enforcement ### [FARASTAR Pulsed Field Ablation Generator, Product ID M004PFCE61M401; Percutaneous Cardiac Ablation Catheter](https://isitonrecall.com/recall/fda-device-z-2751-2026-farastar-pulsed-field-ablation-generator-product-id-m004pfce61m401-percutaneous-cardiac-ablation-cat/) Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information. Class II Reported ongoing Distribution: International distribution in the states of Austria, Spain, France, Germany, Denmark, Italy, Portugal, Great Britain, Ireland. [Official source for FARASTAR Pulsed Field Ablation Generator, Product ID M004PFCE61M401; Percutaneous Cardiac Ablatio...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2751-2026%22) Jun 11, 2026 FDA device enforcement ### [FARASTAR PFA Generator, Product ID M004PFCE61M460; Percutaneous Cardiac Ablation Catheter](https://isitonrecall.com/recall/fda-device-z-2752-2026-farastar-pfa-generator-product-id-m004pfce61m460-percutaneous-cardiac-ablation-catheter/) Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information. Class II Reported ongoing Distribution: International distribution in the states of Austria, Spain, France, Germany, Denmark, Italy, Portugal, Great Britain, Ireland. [Official source for FARASTAR PFA Generator, Product ID M004PFCE61M460; Percutaneous Cardiac Ablation Catheter](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2752-2026%22) Jun 11, 2026 FDA device enforcement ### [FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401; Percutaneous Cardiac Ablation Catheter](https://isitonrecall.com/recall/fda-device-z-2753-2026-farastar-ablation-generator-eu-pulsed-field-ablation-generator-product-id-61m401-percutaneous-cardia/) Boston Scientific is replacing specific FARASTAR PFA generators which have a configuration that is not compatible for use with the FARAPOINT PFA catheter. Class II Reported ongoing Distribution: International distribution in the countries of Italy, Austria, France, Germany, Belgium. [Official source for FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401; Percutaneous ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2753-2026%22) Jun 11, 2026 FDA device enforcement ### [FARADRIVE Steerable Sheath Clear IDE, used to facilitate access to the vasculature and into the chambers of the heart, Material Number 21C602, IFU Reference Number 51636751-01](https://isitonrecall.com/recall/fda-device-z-2754-2026-faradrive-steerable-sheath-clear-ide-used-to-facilitate-access-to-the-vasculature-and-into-the-chamb/) Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to dilator insertion orientation during device preparation. Valve damage may result in air ingress, pote... Class II Reported ongoing Distribution: Global Distribution. US Nationwide. [Official source for FARADRIVE Steerable Sheath Clear IDE, used to facilitate access to the vasculature and into the c...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2754-2026%22) Jun 11, 2026 FDA device enforcement ### [FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the vasculature and into the chambers of the heart, Material Number 21M402, IFU Reference Number LBL1062](https://isitonrecall.com/recall/fda-device-z-2755-2026-faradrive-steerable-sheath-clear-used-to-facilitate-access-to-the-vasculature-and-into-the-chambers/) Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to dilator insertion orientation during device preparation. Valve damage may result in air ingress, pote... Class II Reported ongoing Distribution: Global Distribution. US Nationwide. [Official source for FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the vasculature and into the chamb...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2755-2026%22) Jun 11, 2026 FDA device enforcement ### [FARADRIVE STEERABLE SHEATH (CLEAR) - US, used to facilitate access to the vasculature and into the chambers of the heart, Material Number M004PF21M402, IFU Reference Number 5165...](https://isitonrecall.com/recall/fda-device-z-2756-2026-faradrive-steerable-sheath-clear-us-used-to-facilitate-access-to-the-vasculature-and-into-the-chambe/) Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to dilator insertion orientation during device preparation. Valve damage may result in air ingress, pote... Class II Reported ongoing Distribution: Global Distribution. US Nationwide. [Official source for FARADRIVE STEERABLE SHEATH (CLEAR) - US, used to facilitate access to the vasculature and into th...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2756-2026%22) ## Reasons in these listed records - There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification of an AF Burden Alert may delay clinical evaluation or therapeutic intervention of an atrial arrhythmia. - A subset of power adapters used with the connect console may exhibit higher-than-expected resistance in the electrical grounding path. As a result, the power adaptor may fail electrical safety testing during installation. - Device may fail to deploy the cinch implant and/or fail to cut the suture as intended. - Potential for arterial sheath tip separation or partial tip separation during use. These examples come from this result page and are not a ranking of every recall reason. ## Checking Boston Scientific Corporation ### Is there a recall on boston scientific corporation right now? This archive contains 354 records, including 352 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 Boston Scientific Corporation](https://isitonrecall.com/check/?q=Boston%20Scientific%20Corporation) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)