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Baxter Healthcare Corp. recalls Baxter MiniCap with Povidone-Iodine Solution, 5C4466P, Baxter Healthcare Corporation. For dialysis.
Recalled July 23, 2014 · FDA recall Z-2074-2014 · Baxter Healthcare
Hazard
Inadequate iodine and packaging related defects. · FDA Class II
Units
585,360 units
Sold at
Distributed USA (nationwide) and Canada.
Description
Inadequate iodine and packaging related defects.
Product
Baxter MiniCap with Povidone-Iodine Solution, 5C4466P, Baxter Healthcare Corporation. For dialysis.
Manufacturer(s)
Baxter Healthcare Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →