Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Baxter Recalled by Baxter Healthcare Corp. Due to the white printed paper layer on the pouch...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Baxter Healthcare Corp. directly.
Affected Products
Baxter, MiniCap with Povidone-Iodine solution, 5C4466P. For dialysis.
Quantity: 20,940 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 7 states: AL, AR, KS, MS, MO, TN, TX
About Baxter Healthcare Corp.
Baxter Healthcare Corp. has 126 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report