Key Takeaway

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 by GlaxoSmithKline, LLC. was recalled on October 24, 2012. The hazard: Product Lacks Stability: These lots are being recalled due to the failure to meet the particle size distribution specification.

FDA Drug Class III Terminated

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

Recalled: October 24, 2012 ~310,964 Aerosol Units units affected D-064-2013

Description

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.

Hazard / Reason

Product Lacks Stability: These lots are being recalled due to the failure to meet the particle size distribution specification.

Class III: Product that is not likely to cause adverse health consequences.

Class III is the least severe classification. The product is unlikely to cause adverse health consequences but still violates FDA regulations.

Products Affected

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

Drugs

Company Information

GlaxoSmithKline, LLC.

Zebulon, NC, United States

View all 20 recalls by GlaxoSmithKline, LLC. →

Distribution

Nationwide and Puerto Rico.

Related Recalls

Frequently Asked Questions

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Compare the model number, lot code, serial number, or date range listed in the recall notice with the information on your product's label or packaging. For vehicles, check your VIN at NHTSA.gov/Recalls.

What remedy is available for this recall?

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