Baxter Healthcare Corp. recalls Baxter Amia Automated PD systems are used in the treatment of adult renal failure patients to perform automated peritone

Recalled January 14, 2015 · FDA recall Z-0932-2015 · Baxter Healthcare

Hazard

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

Units

55 units

Sold at

Nationwide Distribution including GA, MA, NC, NY, PA, and WA.

Description

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

Product

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

Manufacturer(s)

Baxter Healthcare Corp.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →