Reported Mar 15, 2023 · Ongoing
Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution, 5C4466P; Accessory to disposable administration set for…
Baxter Healthcare Corporation
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 Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625
Is this the product you have?
- Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution, 5C4466P; Accessory to disposable administration set for peritoneal dialysis
- Lot codes and dates
6 of 6 products
Products covered by this recall Model / number Barcodes Product as published — 00085412007694UDI/DI 00085412007694, Lot numbers: GD912051, exp 31-Mar-2024 — GD912068, exp 30-Apr-2024 — GD912099, exp 30-Apr-2024 — GD912112, exp 30-Apr-2024 — GD912143, exp 30-Apr-2024 5C4466PGD912204, exp 31-May-2024. Expansion on 05/10/2023: with all lots numbers manufactured prior to 09/30/2022. - Amount recalled
- 33,866,400 units
Where it was sold
- Nationwide
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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