Micro Therapeutics, Inc. recalls
Every recall we track for Micro Therapeutics, Inc. — 12 in all, from 2021–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Micro Therapeutics, Inc. peaked in 2022 (3); 12 since 2017.
All FDA recall records for Micro Therapeutics, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 2 | 0 | 2 |
| 2022 | 0 | 0 | 2 | 1 | 3 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 2 | 0 | 2 |
| 2025 | 0 | 2 | 0 | 0 | 2 |
| 2026 (to date) | 0 | 0 | 3 | 0 | 3 |
What to do if you have a recalled Micro Therapeutics, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Micro Therapeutics, Inc. recalls
7 shown- Lower riskMedical device
Micro Therapeutics, Inc. recalls Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code: 00763000448806 he Pipeline Flex
Micro Therapeutics recalls 2 units of Pipeline Flex Embolization Device with Shield Technology (UDI-DI: 00763000448806) due to incorrect diameter labeling. Product is labeled 2.50mm but should be 3.00mm.
Micro TherapeuticsJun 25, 2026 - Lower riskMedical device
Micro Therapeutics, Inc. recalls Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 20 mm 027 REF PED2-300-20. Intracranial aneurysm
Micro Therapeutics recalls Pipeline Flex Embolization Devices with incorrect labeling that may cause improper use in intracranial aneurysm treatment.
Micro TherapeuticsJun 8, 2026 - Use cautionMedical device
Micro Therapeutics, Inc. recalls Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-021-350-16, PED3-021-250-14,
Medtronic Pipeline Vantage Embolization Device with Shield Technology (REFs PED3-021-350-16, etc.) may cause incomplete wall apposition and braid deformation (fish-mouthing) in procedures ≥4mm diameter, potentially leading to thrombosis. Higher risk in women ≤45 years. Check product codes for recall.
Micro TherapeuticsJan 30, 2025 - Lower riskMedical device
Micro Therapeutics, Inc. recalls The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible, single-lumen, end hole catheter designed for the
Micro Therapeutics recalls Apollo Onyx Delivery Microcatheter (AOMC) sold in US with different indications for use than European version. This may lead to improper medical use. Contact for details.
Micro TherapeuticsJan 11, 2024 - UnratedMedical device
Micro Therapeutics, Inc. recalls Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only
Micro Therapeutics recalls sterile Echelon-14 microcatheters (REF 145-5092150) due to potential packaging exposure during transport. Affected units may have wet substance in outer carton.
Micro TherapeuticsJun 30, 2022 - Lower riskMedical device
Micro Therapeutics, Inc. recalls AXIUM DETACHABLE COIL SYSTEM REF QC-4-12-HELIX; Axium Detachable Coil System REF QC-10-30-3D;
Micro Therapeutics recalls two Axium Detachable Coil System models due to incorrect size and configuration labeling, which may lead to improper use. Affected units include QC-4-12-HELIX and QC-10-30-3D with specific lot numbers.
Micro TherapeuticsApr 27, 2022 - Lower riskMedical device
Micro Therapeutics Inc, recalls EV3 Pipeline Flex Embolization Device with Flex Shield Technology
Micro Therapeutics recalls EV3 Pipeline Flex Embolization Device with Flex Shield Technology (PED2-250-10 to PED2-500-35) with specific lot numbers due to potential push wire fractures in the delivery system during use.
Micro TherapeuticsJul 13, 2021
Micro Therapeutics, Inc. recall questions
How many recalls has Micro Therapeutics, Inc. had?
12 recalls from Micro Therapeutics, Inc. are on record with U.S. safety agencies, from 2021–2026.
What is the most recent Micro Therapeutics, Inc. recall?
Micro Therapeutics, Inc. recalls Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code: 00763000448806 he Pipeline Flex, dated Jun 25, 2026. Every Micro Therapeutics, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Micro Therapeutics, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Micro Therapeutics, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.