Baxter Healthcare Corp.: Medical Device Recall in 2014 - (Recall #: Z-2074-2014)

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, Baxter Healthcare Corporation. For dialysis.

Product Classification:

Class II

Date Initiated: June 17, 2014

Date Posted: July 23, 2014

Recall Number: Z-2074-2014

Event ID: 68590

Reason for Recall:

Inadequate iodine and packaging related defects.

Status: Terminated

Product Quantity: 585,360 units

Code Information:

GD895771

Distribution Pattern:

Distributed USA (nationwide) and Canada.

Voluntary or Mandated:

Voluntary: Firm initiated