Baxter Healthcare Corp.: Medical Device Recall in 2015 - (Recall #: Z-0932-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: April 24, 2014

Date Posted: January 14, 2015

Recall Number: Z-0932-2015

Event ID: 69586

Reason for Recall:

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

Status: Terminated

Product Quantity: 55 units

Code Information:

Product Code: 5C9310

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated