GlaxoSmithKline, LLC. recalls Advair HFA (fluticasone propionate 45 mcg and salmeterol 21 mcg) Inhalation Aerosol, 12g, 120 Metered Actuations, For Or
Recalled December 5, 2012 · FDA recall D-064-2013 · 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
310,964 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 45 mcg and salmeterol 21 mcg) Inhalation Aerosol, 12g, 120 Metered Actuations, For Oral Inhalation with Advair HFA actuator only, Rx only, GlaxoSmithKline, Research Triangle Park, NC 27709, NDC 0173-0715-20.
Manufacturer(s)
GlaxoSmithKline, LLC.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →