FDASeptember 5, 2025device

Flow Re-Direction Endoluminal Devices: FRED 27, REF: FRED5019, FRED5029, FRED4528, FRED4026, FRED5526, FRED4508, FRED5514, FRED3536, FRED3511, FRED5014, FRED3516, MV-F451827; FRED X 27, REF: XFRED4017-MVE, XFRED4528-MVE, MV-F501427X, XFRED4518-MVE, XFRED5526-MVE, XFRED4539-MVE, FREDX5522-PMA, FRE...

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

The hazard

Flow diverter may have a manufacturing issue related to the tantalum length and/or tantalum attachment pattern, which may lead the device to be incompletely open or not properly apposed to the vessel wall, which may necessitate device recapture and withdrawal of the delivery system and microcatheter together. Insufficient apposition could lead to long-term health consequences.

What to do

FDA enforcement status: Ongoing

Brands named

microvention

UPCs

008114250203880084242911716300811425020395008424291171700081142502042500811425021033008424291171940084242911709500842429117187008424291170330084242911700200842429117156

Recall history

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

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