Baxter Healthcare Corp.: Medical Device Recall in 2013 - (Recall #: Z-1565-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Baxter, MiniCap with Povidone-Iodine solution, 5C4466P, Baxter Healthcare Corporation. For dialysis. Intended to isolate the Easy-Lock connector of the solution transfer set.

Product Classification:

Class II

Date Initiated: May 21, 2013

Date Posted: July 3, 2013

Recall Number: Z-1565-2013

Event ID: 65254

Reason for Recall:

leaking pouches

Status: Terminated

Product Quantity: 629,280 units

Code Information:

Lot Number GD893891

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated