FDAJuly 9, 2019device

MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582

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

The hazard

Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.

What to do

FDA enforcement status: Terminated

Brands named

siemens medical solutionssiemenssiemens medical

Recall history

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

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MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582 — Recall Details · AllClear