GlaxoSmithKline, LLC. recalls Advair HFA (fluticasone propionate/salmeterol) Inhalation Aerosol, 45mcg/21 mcg 60 Actuations INST, NDC 0173-0715-22, R
Recalled December 5, 2012 · FDA recall D-065-2013 · GlaxoSmithKline
Hazard
Product Lacks Stability: These lots are being recalled due to the failure to meet the particle size distribution specification. · FDA Class III
Units
18,676 Aerosol Units
Sold at
Nationwide and Puerto Rico.
Description
Product Lacks Stability: These lots are being recalled due to the failure to meet the particle size distribution specification.
Product
Advair HFA (fluticasone propionate/salmeterol) Inhalation Aerosol, 45mcg/21 mcg 60 Actuations INST, NDC 0173-0715-22, Rx only, GlaxoSmithKline, Research Triangle Park, NC 27709.
Manufacturer(s)
GlaxoSmithKline, LLC.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →