RecallRadar

FDA Drug recall D-1336-2015

0.9% Sodium Chloride Injection USP, 50 mL Single Dose VIAFLEX Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015,…

On 2015-08-26 the FDA classified a Class I recall of 0.9% Sodium Chloride Injection USP, 50 mL Single Dose VIAFLEX Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015,… by Baxter Healthcare, citing presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1336-2015
ClassificationClass I
Statusterminated
Initiated2015-07-17
Published2015-08-26
Last updated2026-09-13 11:51 UTC
CompanyBaxter Healthcare
DistributionUS

Product

0.9% Sodium Chloride Injection USP, 50 mL Single Dose VIAFLEX Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product Code 2B1301, NDC 0338-0049-11.

Reason

Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.

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#: P319921, Exp 12/15

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-1336-2015%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.