Baxter Healthcare Corporation: Medical Device Recall in 2021 - (Recall #: Z-0768-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

MiniCap Extended Life PD Transfer Set

Product Classification:

Class II

Date Initiated: November 10, 2020

Date Posted: January 13, 2021

Recall Number: Z-0768-2021

Event ID: 86883

Reason for Recall:

Potential for no-flow and leaks under the twist clamp.

Status: Terminated

Product Quantity: 72,771 units

Code Information:

Product Code: 5C4482, UDI: 00085412007731, Lot#, Expiration Date: H20D13100, 4/13/2025; H20D27084, 4/27/2025; H20D30070, 4/30/2025; H20E13107, 5/13/2025; H20E19054, 5/19/2025; H20E22082, 5/22/2025; H20F09061, 6/9/2025; H20F15050, 6/15/2025; H20F18070, 6/18/2025; H20F24086, 6/24/2025; H20F29051, 6/29/2025; H20G13046, 7/13/2025; H20G27087, 7/27/2025; H20G30065, 7/30/2025; H20H05057, 8/5/2025; H20H14067, 8/14/2025; H20H19066, 8/19/2025

Distribution Pattern:

Worldwide and US (Nationwide), Canada, Brazil, Mexico, Bermuda, and Indonesia

Voluntary or Mandated:

Voluntary: Firm initiated