RecallRadar

FDA Drug recall D-1054-2014

Cefepime for Injection USP and Dextrose Injection USP, in Duplex Drug Delivery System, 1 g in 50 mL duplex container, For IV Use Only, Sing…

On 2014-02-12 the FDA classified a Class I recall of Cefepime for Injection USP and Dextrose Injection USP, in Duplex Drug Delivery System, 1 g in 50 mL duplex container, For IV Use Only, Sing… by B Braun Medical, citing presence of Particulate Matter: The 1g Cefepime for Injection USP and Dextrose Injection USP lot has been found to contain visible organic particulate matter in a reserve sample u….

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1054-2014
ClassificationClass I
Statusterminated
Initiated2013-10-15
Published2014-02-12
Last updated2026-09-13 11:51 UTC
CompanyB Braun Medical
DistributionUS

Product

Cefepime for Injection USP and Dextrose Injection USP, in Duplex Drug Delivery System, 1 g in 50 mL duplex container, For IV Use Only, Single Dose, Sterile/Non pyrogenic, Rx Only, B Braun Medical Inc., NDC 0264-3193-11

Reason

Presence of Particulate Matter: The 1g Cefepime for Injection USP and Dextrose Injection USP lot has been found to contain visible organic particulate matter in a reserve sample unit.

Identifiers

ndc0264-3193-11
ndc0264-3195-11
code_infoLot H3A744, Exp 01/15

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-1054-2014%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.