RecallRadar

FDA Drug recall D-0387-2015

Vancomycin Hydrochloride for Injection, USP, 500 mg Sterile Powder per Fliptop Vial, packaged in 10 Units per carton, Rx only, Hospira, Inc…

On 2015-02-25 the FDA classified a Class II recall of Vancomycin Hydrochloride for Injection, USP, 500 mg Sterile Powder per Fliptop Vial, packaged in 10 Units per carton, Rx only, Hospira, Inc… by Hospira, citing temperature Abuse: Products experienced uncontrolled temperature excursions during transit.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0387-2015
ClassificationClass II
Statusterminated
Initiated2014-10-06
Published2015-02-25
Last updated2026-09-13 11:51 UTC
CompanyHospira
DistributionUS

Product

Vancomycin Hydrochloride for Injection, USP, 500 mg Sterile Powder per Fliptop Vial, packaged in 10 Units per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4332-01.

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_infoOne shipment of Lot #: 34-366-8E02; Exp 1OCT2015 to The Harvard Drug Group, Livonia, MI

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-0387-2015%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.