Drug recall
Ventolin HFA (albuterol sulfate) Inhalation Aerosol 90 mcg per actuation, 200 Metered Inhalations, FOR ORAL…
FDA recall event 62799 · Class II · GlaxoSmithKline Inc
Key facts
| Event ID | 62799 |
|---|---|
| Recall numbers | D-1666-2012 |
| Recalling firm | GlaxoSmithKline Inc |
| Product type | Drugs |
| Products | Ventolin HFA (albuterol sulfate) Inhalation Aerosol 90 mcg per actuation, 200 Metered Inhalations, FOR ORAL INHALATION ONLY - For use with Ventolin HFA actuator only. Net. wt. 18 g Rx only… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Does Not Deliver Proper Metered Dose: Potential content of albuterol per dose is below specification. |
| Initiation date | Jul 26, 2012 |
| Report date | Sep 5, 2012 |
| Termination date | Sep 4, 2014 |
| City | Zebulon |
| State | NC |
| Country | United States |
| FEI number | 1033964 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: