RecallRadar

FDA Drug recall D-1326-2015

0.9% Sodium Chloride Injection USP, 500 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation Deerfield, IL 60015, NDC 0338-0049-03

On 2015-08-19 the FDA classified a Class II recall of 0.9% Sodium Chloride Injection USP, 500 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation Deerfield, IL 60015, NDC 0338-0049-03 by Baxter Healthcare, citing presence of Particulate Matter and Lack of Assurance of Sterility: The firm received a complaint for customer of presence of particulate matter, leaky containers, and missing port….

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1326-2015
ClassificationClass II
Statusterminated
Initiated2015-07-02
Published2015-08-19
Last updated2026-09-13 11:51 UTC
CompanyBaxter Healthcare
DistributionTN, TX

Product

0.9% Sodium Chloride Injection USP, 500 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation Deerfield, IL 60015, NDC 0338-0049-03.

Reason

Presence of Particulate Matter and Lack of Assurance of Sterility: The firm received a complaint for customer of presence of particulate matter, leaky containers, and missing port protectors.

Identifiers

ndc0338-0049-01
ndc0338-0049-02
ndc0338-0049-03
ndc0338-0049-04
ndc0338-0049-10
ndc0338-0049-41
ndc0338-0049-11
ndc0338-0049-31
ndc0338-0049-48
ndc0338-0049-18
ndc0338-0049-38
ndc0338-0043-03
ndc0338-0043-04
code_infoLot #: C964601, Exp 4/30/2016

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-1326-2015%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.