FDAFDA · Food and drugs·Recall number Z-2074-2014
Baxter MiniCap with Povidone-Iodine Solution, 5C4466P, Baxter Healthcare Corporation. For dialysis.
Published July 23, 2014 · Recall initiated: June 17, 2014
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
Inadequate iodine and packaging related defects.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Baxter Healthcare Corp.
- Distributor
- Distributed USA (nationwide) and Canada.
- Lot
- GD895771
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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