Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Baxter MiniCap with Povidone-Iodine Solution Recalled by Baxter Healthcare Corp. Due to Inadequate iodine and packaging related defects.
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, Baxter Healthcare Corporation. For dialysis.
Quantity: 585,360 units
Why Was This Recalled?
Inadequate iodine and packaging related defects.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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