Baxter Healthcare Corp.: Medical Device Recall in 2015 - (Recall #: Z-1269-2015)

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:

MiniCap with Povidone-Iodine Solution, item number 5C4466P, for hemodialysis.

Product Classification:

Class II

Date Initiated: January 22, 2015

Date Posted: March 25, 2015

Recall Number: Z-1269-2015

Event ID: 70512

Reason for Recall:

Product may have separating or protruding sponges

Status: Completed

Product Quantity: 4,391,520 units

Code Information:

Lot Numbers: GD896845, Exp. 10/2015; GD897371, Exp. 01/2016; GD896936, Exp. 10/2015; GD897124, Exp. 11/2015; GD897165, Exp. 12/2015; GD897157, Exp. 12/2015; GD896944, Exp. 11/2015; GD896837, Exp. 10/2015

Distribution Pattern:

Worldwide Distribution - Nationwide Distribution and to the countries of : Canada, Austria, Norway, Portugal, Saudi Arabia and Spain.

Voluntary or Mandated:

Voluntary: Firm initiated