Microvention recalls

Microvention has 38 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 19 Aug 2026. 11 are still ongoing. 3 were reported in the last 12 months. The most frequent reason is sterility.

Total recalls38since 2017

Last 12 months3reported

Class I00% of total

Ongoing11latest 19 Aug 2026

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 1Jan '25 1 0 0Apr 0 0 0Jul 1 0 1Oct 0 0 0Jan '26 0 0 0Apr 1 0 0Jul 1 0

Severity split

Class I 0 0%Class II 35 92%Class III 3 8%

Why microvention is recalled

Product types

By year

202625%
2025411%
202425%
202325%
202213%
2021411%
20202258%
201713%

Ongoing microvention recalls

11 active

Reported	Class	Recall	Company	Reason	Where
19 Aug 2026Device	CLASS II	Bobby Balloon Guide Catheter recalled by Microvention	Microvention	Device Malfunction	Nationwide
20 May 2026Device	CLASS II	LVIS Intraluminal Support Device recalled by Microvention	Microvention	Lead & Heavy Metals	Nationwide
22 Oct 2025Device	CLASS II	Flow Re-Direction Endoluminal Devices: FRED recalled by Microvention	Microvention	Lead & Heavy Metals	Nationwide
6 Aug 2025Device	CLASS II	Lifepearl Drug Elutable Microspheres: 200 +/- 50 micrometers recalled	Microvention	Lead & Heavy Metals	GA
19 Feb 2025Device	CLASS II	MicoVention Terumo, LVIS Intraluminal Support Device recalled	Microvention	Sterility	CA
29 Jan 2025Device	CLASS II	Headway" 17 Advanced Straight Microcatheter with Hydrophilic Coating recalled	Microvention	Sterility	CA

All microvention recalls, newest first

38 total

Reported	Class	Recall	Company	Reason	Where
19 Aug 2026Device	CLASS II	Bobby Balloon Guide Catheter recalled by Microvention	Microvention	Device Malfunction	Nationwide
20 May 2026Device	CLASS II	LVIS Intraluminal Support Device recalled by Microvention	Microvention	Lead & Heavy Metals	Nationwide
22 Oct 2025Device	CLASS II	Flow Re-Direction Endoluminal Devices: FRED recalled by Microvention	Microvention	Lead & Heavy Metals	Nationwide
6 Aug 2025Device	CLASS II	Lifepearl Drug Elutable Microspheres: 200 +/- 50 micrometers recalled	Microvention	Lead & Heavy Metals	GA
19 Feb 2025Device	CLASS II	MicoVention Terumo, LVIS Intraluminal Support Device recalled	Microvention	Sterility	CA
29 Jan 2025Device	CLASS II	Headway" 17 Advanced Straight Microcatheter with Hydrophilic Coating recalled	Microvention	Sterility	CA
25 Sep 2024Device	CLASS II	ERIC Retrieval Device recalled by Microvention	Microvention	Other	Nationwide
7 Feb 2024Device	CLASS II	Terumo HydroPearl Compressible Microspheres for Embolisation recalled	Microvention	Other	Nationwide
8 Nov 2023Device	CLASS II	AZUR CX 35 Peripheral Coil System Detachable recalled by Microvention	Microvention	Packaging Defects	Nationwide
2 Aug 2023Device	CLASS II	FRED Flow Re-Direction Endoluminal Device recalled by Microvention	Microvention	Device Malfunction	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.