RecallRadar

FDA Drug recall D-0626-2017

Ventolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 Metered Inhalations, Net Wt. 18 g inhalers, Rx only, GlaxoSm…

On 2017-04-12 the FDA classified a Class II recall of Ventolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 Metered Inhalations, Net Wt. 18 g inhalers, Rx only, GlaxoSm… by Glaxosmithkline, citing defective Delivery System: Elevated number of units with out of specification results for leak rate.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0626-2017
ClassificationClass II
Statusongoing
Initiated2017-03-22
Published2017-04-12
Last updated2026-09-13 11:51 UTC
CompanyGlaxosmithkline
DistributionUS

Product

Ventolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 Metered Inhalations, Net Wt. 18 g inhalers, Rx only, GlaxoSmithKline, Research Triangle Park, NC 22709, NDC 0173-0682-20.

Reason

Defective Delivery System: Elevated number of units with out of specification results for leak rate.

Identifiers

ndc0173-0682-20
ndc0173-0682-24
code_infoLot #: 6ZP9848, Exp 03/18; 6ZP0003, 6ZP9944, Exp 04/18.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0626-2017%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.