Reported Mar 25, 2015 · Completed

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

Baxter Healthcare Corp.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Baxter Healthcare Corp. · 1 Baxter Pkwy · Deerfield, IL · 60015-4625

Is this the product you have?

  • MiniCap with Povidone-Iodine Solution, item number 5C4466P, for hemodialysis.
Lot codes and dates
  • 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
Amount recalled
4,391,520 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

Product may have separating or protruding sponges

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:30 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.