FDAJanuary 30, 2025device

Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-021-350-16, PED3-021-250-14, PED3-021-350-20, PED3-021-250-20, PED3-021-300-16, PED3-021-300-20, PED3-021-275-12, PED3-021-275-16, PED3-021-325-12, PED3-021-325-14, PED3-021-325-16, PED3-021-325-20, PED3-021-250-12, ...

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

The hazard

Use of embolization device with diameters greater-than-or-equal-to 4mm may lead to incomplete wall apposition and/or braid deformation (fish-mouthing/braid narrowing/braid collapse) noted during procedure and post-procedure, typically noted at 6-12 month imaging follow-up, potentially can lead to thrombosis and/or serious adverse events. Higher risk in females less-than-or-equal-to 45 years of age

What to do

FDA enforcement status: Ongoing

Brands named

micro therapeuticsmicro

UPCs

008475360307010084753603519500847536036529008475360304110084753603490700847536036239008475360307250084753603521800847536036543008475360304420084753603493800847536036260

Recall history

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

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