0.9% Sodium Chloride Injection, USP, 500 mL, VIAFLEX Plastic Container, Baxter Healthcare Corporation, Deerfield, IL NDC 0338-0049-03
Reported: September 17, 2014 Initiated: July 30, 2014 #D-1583-2014
Product Description
0.9% Sodium Chloride Injection, USP, 500 mL, VIAFLEX Plastic Container, Baxter Healthcare Corporation, Deerfield, IL NDC 0338-0049-03
Reason for Recall
Lack of Assurance of Sterility; complaints of mold in the overpouch
Details
- Recalling Firm
- Baxter Healthcare Corp.
- Units Affected
- 157,080 containers
- Distribution
- Nationwide
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
0.9% Sodium Chloride Injection, USP, 500 mL, VIAFLEX Plastic Container, Baxter Healthcare Corporation, Deerfield, IL NDC 0338-0049-03. Recalled by Baxter Healthcare Corp.. Units affected: 157,080 containers.
Why was this product recalled? ▼
Lack of Assurance of Sterility; complaints of mold in the overpouch
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 17, 2014. Severity: Moderate. Recall number: D-1583-2014.
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