0.9% Sodium Chloride Injection USP, MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product Code 2B0043, NDC 0338-0553-18.
Reported: June 1, 2016 Initiated: January 21, 2016 #D-0862-2016
Product Description
0.9% Sodium Chloride Injection USP, MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product Code 2B0043, NDC 0338-0553-18.
Reason for Recall
Presence of Particulate Matter: identified as cardboard.
Details
- Recalling Firm
- Baxter Healthcare Corp.
- Units Affected
- 273,520 bags
- Distribution
- Nationwide and Puerto Rico
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
0.9% Sodium Chloride Injection USP, MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product Code 2B0043, NDC 0338-0553-18.. Recalled by Baxter Healthcare Corp.. Units affected: 273,520 bags.
Why was this product recalled? ▼
Presence of Particulate Matter: identified as cardboard.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 1, 2016. Severity: Critical. Recall number: D-0862-2016.
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