FDAOctober 21, 2021device

ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110

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

The hazard

If the system experiences an overvoltage / power surge it can cause a short circuit condition within the Main- cabinet. If this issue occurs, the user may experience an electrical fire within the cabinet, see or smell smoke emitting from the cabinet, or hear a popping sound coming from the cabinet.

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

0088483808561900884838103221

Recall history

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

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