FDAApril 24, 2014device

Baxter Amia Automated PD systems are used in the treatment of adult renal failure patients to perform automated peritoneal dialysis.

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

The hazard

System error 01779 is produced when the battery cannot be charged due to specific voltage differences between the battery and the charger.

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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