Baxter recall
Baxter, MiniCap with Povidone-Iodine solution, 5C4466P. For dialysis.
Why was Baxter recalled?
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 should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Numbers: GD894535, GD894550
- Product
- Baxter, MiniCap with Povidone-Iodine solution, 5C4466P. For dialysis.
- Recalling firm
- Baxter Healthcare Corp.
- Quantity
- 20,940 units
- Distribution
- Distributed in the states of AR, TN MO, KS, TX, MS, and AL.
- Recall date
- July 9, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)