PlainRecalls
FDA Drug Moderate Class II Terminated

5% Dextrose Injection, USP, 1000mL in VIAFLEX Plastic Container, Rx only, Manufactured by Baxter Healthcare Corp., North Cove, North Carolina Facility Highway 221 North, Marion, NC 28752 for Baxter Healthcare Corporation, One Baxter Parkway, Deerfield, IL 60015. NDC 0338-0017-04

Reported: April 1, 2015 Initiated: March 18, 2015 #D-0426-2015

Product Description

5% Dextrose Injection, USP, 1000mL in VIAFLEX Plastic Container, Rx only, Manufactured by Baxter Healthcare Corp., North Cove, North Carolina Facility Highway 221 North, Marion, NC 28752 for Baxter Healthcare Corporation, One Baxter Parkway, Deerfield, IL 60015. NDC 0338-0017-04

Reason for Recall

Lack of Assurance of Sterility. Complaints were receive of missing closures and/or leaks which may compromise product sterility.

Details

Recalling Firm
Baxter Healthcare Corp.
Units Affected
48,874
Distribution
Nationwide
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
5% Dextrose Injection, USP, 1000mL in VIAFLEX Plastic Container, Rx only, Manufactured by Baxter Healthcare Corp., North Cove, North Carolina Facility Highway 221 North, Marion, NC 28752 for Baxter Healthcare Corporation, One Baxter Parkway, Deerfield, IL 60015. NDC 0338-0017-04. Recalled by Baxter Healthcare Corp.. Units affected: 48,874.
Why was this product recalled?
Lack of Assurance of Sterility. Complaints were receive of missing closures and/or leaks which may compromise product sterility.
Which agency issued this recall?
This recall was issued by the FDA Drug on April 1, 2015. Severity: Moderate. Recall number: D-0426-2015.