RecallRadar

FDA Drug recall D-0426-2015

5% Dextrose Injection, USP, 1000mL in VIAFLEX Plastic Container, Rx only, Manufactured by Baxter Healthcare Corp., North Cove, North Caroli…

On 2015-04-01 the FDA classified a Class II recall of 5% Dextrose Injection, USP, 1000mL in VIAFLEX Plastic Container, Rx only, Manufactured by Baxter Healthcare Corp., North Cove, North Caroli… by Baxter Healthcare, citing lack of Assurance of Sterility. Complaints were receive of missing closures and/or leaks which may compromise product sterility.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0426-2015
ClassificationClass II
Statusterminated
Initiated2015-03-18
Published2015-04-01
Last updated2026-09-13 11:51 UTC
CompanyBaxter Healthcare
DistributionUS

Product

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

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

Identifiers

ndc0338-0017-10
ndc0338-0017-41
ndc0338-0017-11
ndc0338-0017-31
ndc0338-0017-48
ndc0338-0017-18
ndc0338-0017-38
ndc0338-0017-02
ndc0338-0017-03
ndc0338-0017-04
ndc0338-0023-02
ndc0338-0023-03
ndc0338-0023-04
code_infoLot #: C926899, Exp 7/31/2015

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0426-2015%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.