0.9% Sodium Chloride Injection USP, 50 mL Single Dose VIAFLEX Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product Code 2B1301, NDC 0338-0049-11.
Reported: August 26, 2015 Initiated: July 17, 2015 #D-1336-2015
Product Description
0.9% Sodium Chloride Injection USP, 50 mL Single Dose VIAFLEX Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product Code 2B1301, NDC 0338-0049-11.
Reason for Recall
Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.
Details
- Recalling Firm
- Baxter Healthcare Corp.
- Units Affected
- 189,120 bags
- Distribution
- Nationwide
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
0.9% Sodium Chloride Injection USP, 50 mL Single Dose VIAFLEX Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product Code 2B1301, NDC 0338-0049-11.. Recalled by Baxter Healthcare Corp.. Units affected: 189,120 bags.
Why was this product recalled? ▼
Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 26, 2015. Severity: Critical. Recall number: D-1336-2015.
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