Baxter Healthcare Corp.: Medical Device Recall in 2014 - (Recall #: Z-1945-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Baxter, MiniCap with Povidone-Iodine solution, 5C4466P. For dialysis.

Product Classification:

Class II

Date Initiated: July 8, 2013

Date Posted: July 9, 2014

Recall Number: Z-1945-2014

Event ID: 68640

Reason for Recall:

the white printed paper layer on the pouch packaging may not be fully adhered to the pouch foil layer. The upper paper layer may serve as a protective barrier and help support overall packaging.

Status: Terminated

Product Quantity: 20,940 units

Code Information:

Lot Numbers: GD894535, GD894550

Distribution Pattern:

Distributed in the states of AR, TN MO, KS, TX, MS, and AL.

Voluntary or Mandated:

Voluntary: Firm initiated