Baxter Healthcare Corporation: Medical Device Recall in 2017 - (Recall #: Z-1056-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

APD Set with Cassette 3-Prong Peritoneal Dialysis Set Indicated for use in the treatment of patients with renal failure to provide PD fluid exchanges with Baxter HomeChoice PD systems in clinical and home use settings.

Product Classification:

Class II

Date Initiated: December 16, 2016

Date Posted: January 25, 2017

Recall Number: Z-1056-2017

Event ID: 75998

Reason for Recall:

Customer complaints received for the presence of leaks

Status: Terminated

Product Quantity: 8640 eaches

Code Information:

H16F16088

Distribution Pattern:

US only

Voluntary or Mandated:

Voluntary: Firm initiated