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D-0426-2015 Class II Terminated

Recalled by Baxter Healthcare Corp. — Deerfield, IL

FDA drug recall D-0426-2015 was initiated by Baxter Healthcare Corp. on Mar 18, 2015 and is designated Class II. Reason for recall: Lack of Assurance of Sterility. Complaints were receive of missing closures and/or leaks which may compromise product sterility. The recall status is terminated (terminated Feb 24, 2016). Affected quantity: 48,874.

Recall Details

Product Type: Drugs
Report Date: Apr 1, 2015
Initiation Date: Mar 18, 2015
Termination Date: Feb 24, 2016
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 48,874

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.

Distribution Pattern

Nationwide

Code Information

Lot #: C926899, Exp 7/31/2015

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-0426-2015
openFDA file date: Oct 27, 2026
Loaded by RegDataLab: Oct 29, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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