Baxter MiniCap with Povidone-Iodine Solution recall
Baxter MiniCap with Povidone-Iodine Solution, 5C4466P, Baxter Healthcare Corporation. For dialysis.
Why was Baxter MiniCap with Povidone-Iodine Solution recalled?
Inadequate iodine and packaging related defects.
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?
GD895771
- Product
- Baxter MiniCap with Povidone-Iodine Solution, 5C4466P, Baxter Healthcare Corporation. For dialysis.
- Recalling firm
- Baxter Healthcare Corp.
- Quantity
- 585,360 units
- Distribution
- Distributed USA (nationwide) and Canada.
- Recall date
- July 23, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)