Drug recall
Advair Diskus 100/50mcg (fluticasone propionate/salmeterol inhalation powder, 100/50mcg), Expiration Date…
FDA recall event 52986 · Class II · GlaxoSmithKline Inc
Key facts
| Event ID | 52986 |
|---|---|
| Recall numbers | D-1972-2009 |
| Recalling firm | GlaxoSmithKline Inc |
| Product type | Drugs |
| Products | Advair Diskus 100/50mcg (fluticasone propionate/salmeterol inhalation powder, 100/50mcg), Expiration Date: April 2010, Rx only, NDC 0173-0695-00, GlaxoSmithKline, Research Triangle Park, NC 27709. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Defective delivery system; There is a potential for the foil strip of the inhaler to tear rather than to peel back, which can result in medication not being available to the user as they advance doses… |
| Initiation date | Aug 4, 2009 |
| Termination date | Nov 3, 2010 |
| 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