FDAFDA · Food and drugs·Recall number Z-1945-2014
Baxter, MiniCap with Povidone-Iodine solution, 5C4466P. For dialysis.
Published July 9, 2014 · Recall initiated: July 8, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated
Recall details
- Manufacturer
- Baxter Healthcare Corp.
- Distributor
- Distributed in the states of AR, TN MO, KS, TX, MS, and AL.
- Lot
- Lot Numbers: GD894535, GD894550
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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