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Albuterol Sulfate Inhalation Solution (Asthma Medication) Recall
 
On January 3, 2011, the USFDA MedWatch reported that the Ritedose Corporation is conducting a voluntary recall of 0.083% Albuterol Sulfate Inhalation Solution, 3 mL (in 25, 30, and 60 unit dose vials). This product is a prescription inhalation solution, administered via a nebulizer.
The following lot numbers manufactured by The Ritedose Corporation under NDC: 0591-3797-83, 0591-3797-30, and 0591-3797-60 are included in the recall: 0N81, 0N82, 0N83, 0N84, 0NE7, 0NE8, 0NE9, 0NF0, 0P12, 0P13, 0P46, 0P47, 0PF0, and 0S15. No other Albuterol formulations or products are included in this recall.
Below is the link for further information:

http://www.fda.gov/Safety/Recalls/ucm238528.htm.  
The reason for the recall is that the 2.5/3 ml vial has been embossed with the incorrect dosage concentration and could pose a health hazard. 
Consumers are advised to return the Albuterol to the place it was obtained.  Contact information for The Ritedose Corporation is listed below. 
Contact:
The Ritedose Corporation
803-935-3995
recall@ritedose.com
 
 
 
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