--- title: "Micro Therapeutics, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Micro Therapeutics, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/micro-therapeutics-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Micro Therapeutics, Inc. recall records **9** reported ongoing 9 records in this archive. Latest source date Jun 8, 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 8, 2026 FDA device enforcement ### [Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 12 mm 027 REF PED2-300-12. Intracranial aneurysm flow diverter](https://isitonrecall.com/recall/fda-device-z-2773-2026-pipeline-flex-embolization-device-with-shield-technology-3-00-mm-x-12-mm-027-ref-ped2-300-12-intracr/) Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20 mm implants. Class II Reported ongoing Distribution: US Nationwide distribution in the states of CT, DE, IN, MA, NC, NJ, NM, NY, OH, PA, TX, VA, WA. [Official source for Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 12 mm 027 REF PED2-300-12. In...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2773-2026%22) Jun 8, 2026 FDA device enforcement ### [Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 20 mm 027 REF PED2-300-20. Intracranial aneurysm flow diverter](https://isitonrecall.com/recall/fda-device-z-2774-2026-pipeline-flex-embolization-device-with-shield-technology-3-00-mm-x-20-mm-027-ref-ped2-300-20-intracr/) Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20 mm implants. Class II Reported ongoing Distribution: US Nationwide distribution in the states of CT, DE, IN, MA, NC, NJ, NM, NY, OH, PA, TX, VA, WA. [Official source for Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 20 mm 027 REF PED2-300-20. In...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2774-2026%22) Jan 30, 2025 FDA device enforcement ### [Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-027-350-12, PED3-027-350-14, PED3-027-350-16, PED3-027-350-20, PED3-027-350-25, PED3-027-400-12,...](https://isitonrecall.com/recall/fda-device-z-1245-2025-medtronic-pipeline-vantage-embolization-device-with-shield-technology-ref-ped3-027-350-12-ped3-027-3/) Use of embolization device with diameters greater-than-or-equal-to 4mm may lead to incomplete wall apposition and/or braid deformation (fish-mouthing/braid narrowing/braid collapse) noted during procedure and post-procedure, typically noted at 6-12 month im... Class I Reported ongoing Distribution: Worldwide distribution: US (nationwide): PR, OK, CA, MD, FL, NY, WA, MI, AL, NV, MN, NJ, IL, OH, AK, CT, TN, MO, TX, ID, AZ, WI, PA, OR, SD, VA, CO, GA, KY, IN, AR, MA, LA, NE, ... [Official source for Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-027-350-12, PED3...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1245-2025%22) Jan 30, 2025 FDA device enforcement ### [Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-021-350-16, PED3-021-250-14, PED3-021-350-20, PED3-021-250-20, PED3-021-300-16, PED3-021-300-20,...](https://isitonrecall.com/recall/fda-device-z-1246-2025-medtronic-pipeline-vantage-embolization-device-with-shield-technology-ref-ped3-021-350-16-ped3-021-2/) Use of embolization device with diameters greater-than-or-equal-to 4mm may lead to incomplete wall apposition and/or braid deformation (fish-mouthing/braid narrowing/braid collapse) noted during procedure and post-procedure, typically noted at 6-12 month im... Class I Reported ongoing Distribution: Worldwide distribution: US (nationwide): PR, OK, CA, MD, FL, NY, WA, MI, AL, NV, MN, NJ, IL, OH, AK, CT, TN, MO, TX, ID, AZ, WI, PA, OR, SD, VA, CO, GA, KY, IN, AR, MA, LA, NE, ... [Official source for Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-021-350-16, PED3...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1246-2025%22) Jan 11, 2024 FDA device enforcement ### [The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible, single-lumen, end hole catheter designed for the infusion of the Onyx liquid embolic system (LES). The cathet...](https://isitonrecall.com/recall/fda-device-z-1252-2024-the-apollo-onyx-delivery-microcatheter-aomc-is-a-dmso-compatible-single-lumen-end-hole-catheter-desi/) European version of microcatheter were distributed within US which contain a different "Indications for Use". Class II Reported ongoing Distribution: US Nationwide distribution in the states of AL, AZ, CA, CT, FL, GA, HI, IA, IL, IN, KS, MA, MD, MI, MO, NC, ND, NE, NV, NY, OH, OK, PA, SC, TN, TX, UT, VA, WA, WI. [Official source for The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible, single-lumen, end hole cathet...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1252-2024%22) Jan 11, 2024 FDA device enforcement ### [The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible, single-lumen, end hole catheter designed for the infusion of the Onyx liquid embolic system (LES). The cathet...](https://isitonrecall.com/recall/fda-device-z-1253-2024-the-apollo-onyx-delivery-microcatheter-aomc-is-a-dmso-compatible-single-lumen-end-hole-catheter-desi/) European version of microcatheter were distributed within US which contain a different "Indications for Use". Class II Reported ongoing Distribution: US Nationwide distribution in the states of AL, AZ, CA, CT, FL, GA, HI, IA, IL, IN, KS, MA, MD, MI, MO, NC, ND, NE, NV, NY, OH, OK, PA, SC, TN, TX, UT, VA, WA, WI. [Official source for The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible, single-lumen, end hole cathet...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1253-2024%22) Jun 30, 2022 FDA device enforcement ### [Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only](https://isitonrecall.com/recall/fda-device-z-1556-2022-echelon-14-45-tip-shape-ref-145-5092150-sterile-eo-rx-only/) Outer carton packaging of microcatheters were exposed to wet substance during transport. Class II Reported ongoing Distribution: US Nationwide Distribution: None OUS: Brazil [Official source for Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1556-2022%22) Jun 30, 2022 FDA device enforcement ### [Echelon -14 Micro Catheter, REF: 105-5092-150, sterile EO, Rx Only](https://isitonrecall.com/recall/fda-device-z-1557-2022-echelon-14-micro-catheter-ref-105-5092-150-sterile-eo-rx-only/) Outer carton packaging of microcatheters were exposed to wet substance during transport. Class II Reported ongoing Distribution: US Nationwide Distribution: None OUS: Brazil [Official source for Echelon -14 Micro Catheter, REF: 105-5092-150, sterile EO, Rx Only](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1557-2022%22) Apr 27, 2022 FDA device enforcement ### [AXIUM DETACHABLE COIL SYSTEM REF QC-4-12-HELIX; Axium Detachable Coil System REF QC-10-30-3D;](https://isitonrecall.com/recall/fda-device-z-1261-2022-axium-detachable-coil-system-ref-qc-4-12-helix-axium-detachable-coil-system-ref-qc-10-30-3d/) Due to incorrect size and configuration labeling of the detachable coil system. Class II Reported ongoing Distribution: International distribution in the countries of China and Republic of Korea. [Official source for AXIUM DETACHABLE COIL SYSTEM REF QC-4-12-HELIX; Axium Detachable Coil System REF QC-10-30-3D;](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1261-2022%22) ## Reasons in these listed records - Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20 mm implants. - Use of embolization device with diameters greater-than-or-equal-to 4mm may lead to incomplete wall apposition and/or braid deformation (fish-mouthing/braid narrowing/braid collapse) noted during procedure and post-procedure, typically noted at 6-12 month imaging follow-up, pot... - European version of microcatheter were distributed within US which contain a different "Indications for Use". - Outer carton packaging of microcatheters were exposed to wet substance during transport. These examples come from this result page and are not a ranking of every recall reason. ## Checking Micro Therapeutics, Inc. ### Is there a recall on micro therapeutics, inc. right now? This archive contains 9 records, including 9 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 Micro Therapeutics, Inc.](https://isitonrecall.com/check/?q=Micro%20Therapeutics%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)