Baxter MiniCap with Povidone-Iodine Solution, 5C4466P, Baxter Healthcare Corporation. For dialysis.
Reported: July 23, 2014 Initiated: June 17, 2014 #Z-2074-2014
Product Description
Baxter MiniCap with Povidone-Iodine Solution, 5C4466P, Baxter Healthcare Corporation. For dialysis.
Reason for Recall
Inadequate iodine and packaging related defects.
Details
- Recalling Firm
- Baxter Healthcare Corp.
- Units Affected
- 585,360 units
- Distribution
- Distributed USA (nationwide) and Canada.
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
Baxter MiniCap with Povidone-Iodine Solution, 5C4466P, Baxter Healthcare Corporation. For dialysis.. Recalled by Baxter Healthcare Corp.. Units affected: 585,360 units.
Why was this product recalled? ▼
Inadequate iodine and packaging related defects.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 23, 2014. Severity: Moderate. Recall number: Z-2074-2014.
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