MICROVENTION INC. recalls
Every recall we track for MICROVENTION INC. — 38 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from MICROVENTION INC. peaked in 2019 (22); 38 since 2017.
All FDA recall records for MICROVENTION 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 | 1 | 0 | 1 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 21 | 1 | 22 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 4 | 0 | 4 |
| 2022 | 0 | 1 | 0 | 0 | 1 |
| 2023 | 0 | 0 | 1 | 2 | 3 |
| 2024 | 0 | 0 | 2 | 1 | 3 |
| 2025 | 0 | 0 | 2 | 0 | 2 |
| 2026 (to date) | 0 | 1 | 1 | 0 | 2 |
Most common reasons for MICROVENTION INC. recalls
What to do if you have a recalled MICROVENTION 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 MICROVENTION INC. recalls
16 shown- Lower riskMedical device
MICROVENTION INC. recalls BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in
Microvention recalls Bobby Balloon Guide Catheters with serial numbers BOB-895-CN, BOB-895-EMEA, BOB-895-EMEA-AL, BOB-895-US, and MV-BGA01095 due to increased balloon pinhole defects.
MicroventionApr 30, 2026 - Use cautionMedical device
MICROVENTION INC. recalls LVIS Intraluminal Support Device, REF/Outside Diameter(OD)xTotal Length(TL)xWorking Length(WL): 214022-CAS/4.0 mm x 22
Microvention recalls specific LVIS Intraluminal Support Devices due to potential manufacturing errors that could cause vessel injury, rupture, or neurological issues. Affected units include certain sizes and production lots.
MicroventionApr 6, 2026 - Lower riskMedical device
MICROVENTION INC. recalls Flow Re-Direction Endoluminal Devices: FRED 27, REF: FRED5019, FRED5029, FRED4528, FRED4026, FRED5526, FRED4508,
Microvention recalls specific flow re-direction endoluminal devices due to potential incomplete deployment, which could lead to long-term health issues. Affected models include FRED 27 and related references.
MicroventionSep 5, 2025 - Lower riskMedical device
MICROVENTION INC. recalls LIFEPEARL Drug Elutable Microspheres: 200 +/- 50 micrometers, REF: 8LP2S200; 400 +/- 50 micrometers, REF: 8LP2S400
Microvention recalls LIFEPEARL Drug Elutable Microspheres (200/400 micrometers) due to potential inability to reach target treatment areas, requiring additional procedures. Affected units have specific reference numbers.
MicroventionMay 29, 2025 - UnratedMedical device
MICROVENTION INC. recalls MicoVention Terumo, LVIS Intraluminal Support Device, REF: 213522-CAS, od, 3.5 mm, TL 22 mm, WL 18 mm, Sterile R,
MicoVention Terumo recalls specific LVIS Intraluminal Support Devices due to risk of stent not being pushed out of the introducer during use, potentially causing complications.
MicoVention TerumoDec 11, 2024 - Lower riskMedical device
MICROVENTION INC. recalls Microvention, Headway" 17 Advanced Straight Microcatheter with Hydrophilic Coating, REF: MC172150SX-CN, Sterile R, Rx
Microvention recalls specific microcatheter models due to potential incomplete packaging seals that could compromise sterility. Affected units include lot #0000629846. Consumers should contact Microvention for details.
MicroventionDec 2, 2024 - Lower riskMedical device
MICROVENTION INC. recalls ERIC Retrieval Device REF: ER173020 ER174030 ER176044 The ERIC Retrieval Device is a mechanical thrombectomy device
Microvention recalls ERIC Retrieval Devices with incorrect 5-year expiration dates (should be 3 years). Affected models include ER173020, ER174030, and ER176044. Contact for details.
MicroventionAug 5, 2024 - UnratedMedical device
MICROVENTION INC. recalls TERUMO HydroPearl Compressible Microspheres for Embolisation REF 8HP2S600
Microvention recalls HydroPearl Compressible Microspheres (REF 8HP2S600) due to manufacturing defects that may affect safety. Learn if your product is affected and what to do.
MicroventionDec 21, 2023 - Lower riskMedical device
MICROVENTION INC. recalls AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, REF: 45-751324
Microvention recalls AZUR CX 35 Peripheral Coil System Detachable due to potential unsealed pouch packaging. Learn if you have the affected model and what to do.
MicroventionAug 24, 2023 - UnratedMedical device
MICROVENTION INC. recalls FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511, FRED3511-PMA, FRED3516-CA, FRED3516-PMA,
Microvention recalls FRED Flow Re-Direction Endoluminal Devices made between June 1, 2020, and September 29, 2020, due to potential incorrect inner stent length causing improper function.
MicroventionJun 7, 2023 - Use cautionMedical device
MICROVENTION INC. recalls WEB Detachment Controller, REF: WDC-2, WDC, MV-WDC2. Component of WEB Aneurysm Embolization System.
Microvention recalls WEB Detachment Controller (WDC-2) due to potential implant misplacement during aneurysm embolization. Affected units have specific serial numbers sold in China and Japan. Contact for remedy.
MicroventionSep 21, 2022 - Lower riskMedical device
MICROVENTION INC. recalls Aspiration Syringe Kit, REF: MVSK60
Microvention recalls Aspiration Syringe Kit REF MVSK60 shipped to US customers without proper labeling. Affected units have specific lot and UDI codes. Stop using if you have the kit.
MicroventionOct 20, 2021 - Lower riskMedical device
MICROVENTION INC. recalls VIA Microcatheter VIA 21 REF VIA-21-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a
Microvention recalls VIA Microcatheter VIA 21 REF VIA-21-154-01 due to international labeling differences that may cause confusion with US-cleared labels.
MicroventionApr 21, 2021 - Lower riskMedical device
Microvention, Inc. recalls Terumo AZUR CX Peripheral Coil System, Detachable 35, CX Coil, REF numbers 45-751019, 45-751324, 45-751632, 45-752039,
Microvention recalls AZUR CX Peripheral Coil System (detachable 35) with REF numbers 45-751019 to 45-752039 and MV-AX codes. Devices may be missing the implant coil, which could lead to complications.
MicroventionNov 24, 2019 - Lower riskMedical device
Microvention, Inc. recalls MicroVention Terumo HydroSoft 10, HydroCoil Embolic System, Endovascular Embolization Coil, Helical, Sterile, Rx, REF
Microvention recalls HydroSoft 10 and HydroCoil Embolic Systems with missing implant coils. Affected units have specific Rx/REF numbers. Contact Microvention for details.
MicroventionNov 22, 2019 - Lower riskMedical device
Microvention, Inc. recalls MicroVention Terumo Traxcess 7 Mini Guidewire with Hydrophilic Coating, Ref GW0721006M, 1 guidewire per package,
Microvention recalls Traxcess 7 Mini Guidewires with hydrophilic coating that may delaminate. Affected units have specific lot numbers. Contact for remedy.
MicroventionAug 7, 2017
MICROVENTION INC. recall questions
How many recalls has MICROVENTION INC. had?
38 recalls from MICROVENTION INC. are on record with U.S. safety agencies, from 2017–2026.
What is the most recent MICROVENTION INC. recall?
MICROVENTION INC. recalls BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in, dated Apr 30, 2026. Every MICROVENTION INC. recall is listed on this page, newest first.
Why are MICROVENTION INC. products recalled?
The most common reasons on record: The devices may be missing the implant coil. (22).
What should I do if I have a recalled MICROVENTION 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 MICROVENTION 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.