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FDAFebruary 1, 2023device

Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution, 5C4466P; Accessory to disposable administration set for peritoneal dialysis

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

MiniCap Disconnect Cap with Povidone-Iodine are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals. This could lead to exposure to air, resulting in insufficient iodine/dry sponge inside the MiniCap, which could lead to the potential for inadequate disinfectant.

What to do

FDA enforcement status: Ongoing

Brands named

baxter healthcarebaxter

UPCs

00085412007694

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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