FDA Drug recall D-0793-2017
Ventolin HFA (albuterol sulfate) Inhalation, 90 mcg per actuation, 200 Metered Inhalations, Net Wt. 18 g inhalers, Rx only, GlaxoSmithKline…
- FDA Drug
- Class II
- ongoing
- Published 2017-05-31
On 2017-05-31 the FDA classified a Class II recall of Ventolin HFA (albuterol sulfate) Inhalation, 90 mcg per actuation, 200 Metered Inhalations, Net Wt. 18 g inhalers, Rx only, GlaxoSmithKline… by Glaxosmithkline, citing defective Delivery System: Elevated number of units with out of specification results for leak rate.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0793-2017 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2017-05-16 |
| Published | 2017-05-31 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Glaxosmithkline |
| Distribution | US |
Product
Ventolin HFA (albuterol sulfate) Inhalation, 90 mcg per actuation, 200 Metered Inhalations, Net Wt. 18 g inhalers, Rx only, GlaxoSmithKline, Research Triangle Park, NC 27709, NDC 0173-0682-20.
Reason
Defective Delivery System: Elevated number of units with out of specification results for leak rate
Identifiers
| ndc | 0173-0682-20 |
|---|---|
| ndc | 0173-0682-24 |
| code_info | Lot#: 7ZP0634, 7ZP0810, 7ZP0990, Exp. 5/18 |
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-0793-2017%22
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