FDANovember 22, 2019device

MicroVention Terumo HydroFrame 18, HydroCoil Embolic System, Endovascular Embolization Coil, Sterile, Rx, REF numbers 180723HFRM-V, 180931HFRM-V, 181644HFRM-V, MV-80619HHFA, MV80827HHFA, MV-80931HHFA, and MV-81036HHFA. Product Usage: The HES is also intended for vascular occlusion of blood vessel...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The devices may be missing the implant coil.

What to do

FDA enforcement status: Terminated

Brands named

microvention

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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