January 3rd, the US FDA MedWatch reported a Ritedose Corporation voluntary recall of 0.083% Albuterol Sulfate Inhalation Solution. Please go to the recall notice for the container sizes and lot numbers recalled http://www.fda.gov/Safety/Recalls/ucm238528.htm.

This product is recalled due to 2.5 mg/3 mL single use vials embossed with the wrong dosage concentration therefore, represents a potential significant health hazard. Consumers should immediately return the affected product to the place it was obtained (i.e. doctor’s office, pharmacy, etc.). For more information, contact Ritedose Corporation 803-935-3995 Monday through Friday 8am to 5 pm EST or: recall@ritedose.com.