RecallRadar

FDA Drug recall D-1179-2016

DEXPANTHENOL 250MG/ML W/PRES. (BENZALKONIUM CHL 0.01%), 10ML Vials, MEDAUS PHARMACY

On 2016-07-20 the FDA classified a Class II recall of DEXPANTHENOL 250MG/ML W/PRES. (BENZALKONIUM CHL 0.01%), 10ML Vials, MEDAUS PHARMACY by Medaus, citing lack of Assurance of Sterility.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1179-2016
ClassificationClass II
Statusterminated
Initiated2016-05-13
Published2016-07-20
Last updated2026-09-13 11:51 UTC
CompanyMedaus
DistributionUS

Product

DEXPANTHENOL 250MG/ML W/PRES. (BENZALKONIUM CHL 0.01%), 10ML Vials, MEDAUS PHARMACY

Reason

Lack of Assurance of Sterility

Identifiers

code_info
Lot #: 160204-45, BUD: 06/14/16; Lot #: 160210-38, BUD: 06/14/16; Lot #: 160215-9, BUD: 06/14/16; Lot #: 160222-16,…Lot #: 160204-45, BUD: 06/14/16; Lot #: 160210-38, BUD: 06/14/16; Lot #: 160215-9, BUD: 06/14/16; Lot #: 160222-16, BUD: 06/14/16; Lot #: 160223-6, BUD: 06/14/16; Lot #: 160229-74, BUD: 06/14/16; Lot #: 160302-31, BUD: 06/14/16; Lot #: 160307-27, BUD: 06/14/16

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-1179-2016%22

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