FDAOctober 21, 2014device

HomeChoice/HomeChoice Pro Automated Personal Cycler, for Automated Peritoneal Dialysis. Product codes 5C8310, 5C8310R, R5C8320, and 5C4474.

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

The hazard

The keypad buttons on HomeChoice devices may be activated without the operator pressing them.

What to do

FDA enforcement status: Terminated

Brands named

baxter healthcarebaxter

Recall history

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

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