FDAJune 12, 2023device

MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)

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

The hazard

During installation of the SmokeDetector Interlock, a connecting cable, between the SmokeDetector Interlock and the host PC, may not have been properly installed. This connection is used for service diagnostics and does not impact the functionality of the system and/or the SmokeDetector Interlock system.

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

0088483810411200884838104402

Recall history

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

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