RecallRadar

FDA Drug recall D-813-2013

Sodium Chloride Injection, USP, 0.9%, 20 mL Single-dose Fliptop Plastic Vial, packaged in 25 vial Units per carton, Rx only, Hospira, Inc.,…

On 2013-07-31 the FDA classified a Class II recall of Sodium Chloride Injection, USP, 0.9%, 20 mL Single-dose Fliptop Plastic Vial, packaged in 25 vial Units per carton, Rx only, Hospira, Inc.,… by Hospira, citing presence of Particulate Matter: Confirmed customer report of visible particulate in the form of an orange or rust colored ring embedded in between the plastic layers of the plasti….

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-813-2013
ClassificationClass II
Statusterminated
Initiated2013-06-27
Published2013-07-31
Last updated2026-09-13 11:51 UTC
CompanyHospira
DistributionUS

Product

Sodium Chloride Injection, USP, 0.9%, 20 mL Single-dose Fliptop Plastic Vial, packaged in 25 vial Units per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-4888-20.

Reason

Presence of Particulate Matter: Confirmed customer report of visible particulate in the form of an orange or rust colored ring embedded in between the plastic layers of the plastic vial.

Identifiers

ndc0409-4888-02
ndc0409-4888-10
ndc0409-4888-03
ndc0409-4888-20
ndc0409-4888-06
ndc0409-4888-50
ndc0409-4888-01
ndc0409-4888-12
ndc0409-4888-90
ndc0409-1918-42
ndc0409-1918-32
ndc0409-1918-43
ndc0409-1918-33
ndc0409-1918-45
ndc0409-1918-35
code_infoLot #: 15-058-DK*, Exp 1MAR2014; note the * may be followed by 01

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-813-2013%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.