RecallRadar

FDA Drug recall D-0390-2015

Vancomycin Hydrochloride for Injection, USP, 1 g Sterile Powder per Fliptop Vial, packaged in 10 Units per carton, Rx only, Hospira Inc., L…

On 2015-02-25 the FDA classified a Class II recall of Vancomycin Hydrochloride for Injection, USP, 1 g Sterile Powder per Fliptop Vial, packaged in 10 Units per carton, Rx only, Hospira Inc., L… by Hospira, citing temperature Abuse: Products experienced uncontrolled temperature excursions during transit.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0390-2015
ClassificationClass II
Statusterminated
Initiated2014-10-06
Published2015-02-25
Last updated2026-09-13 11:51 UTC
CompanyHospira
DistributionUS

Product

Vancomycin Hydrochloride for Injection, USP, 1 g Sterile Powder per Fliptop Vial, packaged in 10 Units per carton, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-6533-01.

Reason

Temperature Abuse: Products experienced uncontrolled temperature excursions during transit.

Identifiers

ndc0409-6531-12
ndc0409-6531-02
ndc0409-6533-11
ndc0409-6533-01
ndc0409-6533-21
ndc0409-4332-11
ndc0409-4332-01
ndc0409-3515-11
ndc0409-3515-01
code_infoLot #: 35-315-DD; Exp 1NOV2015

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-0390-2015%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.