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.

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

Severity split

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

By year

Ongoing microvention recalls

11 active

All microvention recalls, newest first

38 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIBobby Balloon Guide Catheter recalled by MicroventionMicroventionDevice MalfunctionNationwide
DeviceCLASS IILVIS Intraluminal Support Device recalled by MicroventionMicroventionOtherCA
DeviceCLASS IIFlow Re-Direction Endoluminal Devices: FRED recalled by MicroventionMicroventionOtherNationwide
DeviceCLASS IILifepearl Drug Elutable Microspheres: 200 +/- 50 micrometers recalledMicroventionOtherGA
DeviceCLASS IIMicoVention Terumo, LVIS Intraluminal Support Device recalledMicroventionOtherCA
DeviceCLASS IIHeadway" 17 Advanced Straight Microcatheter with Hydrophilic Coating recalledMicroventionSterilityCA
DeviceCLASS IIERIC Retrieval Device recalled by MicroventionMicroventionOtherNationwide
DeviceCLASS IITerumo HydroPearl Compressible Microspheres for Embolisation recalledMicroventionOtherNationwide
DeviceCLASS IIAZUR CX 35 Peripheral Coil System Detachable recalled by MicroventionMicroventionPackaging DefectsNationwide
DeviceCLASS IIFRED Flow Re-Direction Endoluminal Device recalled by MicroventionMicroventionDevice MalfunctionNationwide
DeviceCLASS IIWEB Detachment Controller recalled by MicroventionMicroventionPotency & AssayNationwide
DeviceCLASS IIAspiration Syringe Kit recalled by MicroventionMicroventionOtherNationwide
DeviceCLASS IIIVIA Microcatheter VIA recalled by MicroventionMicroventionOtherNationwide
DeviceCLASS IIIVIA Microcatheter VIA recalled by MicroventionMicroventionOtherNationwide
DeviceCLASS IIIVIA Microcatheter VIA recalled by MicroventionMicroventionOtherNationwide
DeviceCLASS IITerumo Microplex 10, Platinum Coil System recalled by MicroventionMicroventionOtherGA
DeviceCLASS IITerumo Microplex 18, Platinum Coil System recalled by MicroventionMicroventionOtherGA
DeviceCLASS IITerumo HydroSoft 10, HydroCoil Embolic System recalled by MicroventionMicroventionOtherGA
DeviceCLASS IITerumo Microplex 18, Platinum Embolization Coil, Cosmos recalledMicroventionOtherGA
DeviceCLASS IITerumo HydroFrame 10, HydroCoil Embolic System recalled by MicroventionMicroventionOtherGA
DeviceCLASS IITerumo Microplex 10, Platinum Coil System recalled by MicroventionMicroventionOtherGA
DeviceCLASS IITerumo Microplex 10, Platinum Coil System recalled by MicroventionMicroventionOtherGA
DeviceCLASS IITerumo Microplex, Platinum Coil System recalled by MicroventionMicroventionOtherGA
DeviceCLASS IITerumo Microplex 10, Platinum Coil System recalled by MicroventionMicroventionOtherGA
DeviceCLASS IITerumo Microplex 10, Platinum Coil System recalled by MicroventionMicroventionOtherGA
DeviceCLASS IITerumo Microplex 10, Platinum Coil System recalled by MicroventionMicroventionOtherGA
DeviceCLASS IITerumo HydroFrame 18, HydroCoil Embolic System recalled by MicroventionMicroventionOtherGA
DeviceCLASS IITerumo Microplex 18, Platinum Coil System recalled by MicroventionMicroventionOtherGA
DeviceCLASS IITerumo Microplex 10, Platinum Coil System recalled by MicroventionMicroventionOtherGA
DeviceCLASS IITerumo Microplex 18, Platinum Coil System recalled by MicroventionMicroventionOtherGA

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.