FDAApril 8, 2019device

MediPress pneumatic compression system Full Arm (Medium)-Segmental Gradient, Model #6104M-S

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

The hazard

Product design change did not receive proper premarket clearance and lacks a 510 (k)

What to do

FDA enforcement status: Terminated

Brands named

compass health brands corporate officecompasscompass health

Recall history

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

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