FDAOctober 1, 2025device

DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;

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

The hazard

Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems dmcphilipsphilips medical

UPCs

0088483809069900884838090705

Recall history

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

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