FDADecember 29, 2023device

SmartPath to dStream for 1.5T, Model No. 781260, 782112

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

The hazard

An incorrect electrical shock warning label may have been placed on the Liquid Cooling Cabinet (LCC) of affected MR systems. The caution symbol on the incorrect label has a white background instead of yellow, and the label is missing the high voltage warning symbol. This presents a potential risk of electrical shock for service personnel.

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

0088483809507600884838098886

Recall history

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

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SmartPath to dStream for 1.5T, Model No. 781260, 782112 — Recall Details · AllClear