FDAJune 7, 2023device

FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511, FRED3511-PMA, FRED3516-CA, FRED3516-PMA, FRED3524, FRED3524-CA, FRED3524-PMA, FRED3536-CA, FRED3536-PMA, FRED4007-PMA, FRED4012-CA, FRED4012-PMA, FRED4017-PMA, FRED4026, FRED4026-PMA, FRED4038-PMA, FRED4508, FRED4508-PMA, FRE...

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

The hazard

Intracranial aneurysm flow diverter device may be manufactured with an incorrect inner stent length and may not perform as intended.

What to do

FDA enforcement status: Ongoing

Brands named

microvention

UPCs

008424291066550084242910666200842429106679008114250209820084242910668600842429106709008424291067230084242910673000842429106747008424291067540081142502105700842429106761

Recall history

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

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