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Ritedose Corp. is conducting a voluntary recall of albuterol sulfate inhalation solution 0.083%, 3mL in 25, 30, and 60 unit dose vials.
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Voluntary Recall of Ritedose Corporation 0.083% Albuterol Sulfate Inhalation Solution,. 3 mL Unit Dose Vials. On December 30, 2010, the U.S. Food and Drug
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Jan 3, 2011 -- The Ritedose Corporation has recalled some single-dose vials of Albuterol Sulfate Inhalation Solution because an incorrect label
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7, 1994 (301) 443-3285 ALBUTEROL RECALL UPDATE FDA has been receiving inquiries about the voluntary recall by Copley Pharmaceutical Inc. of all lots of
The FDA is warning that dose vials of albuterol distributed by Ritedose are mislabeled and may contain five times the amount of the drug
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The maker of a nebulized asthma treatment recalled several drug lots vials of its 0.083% Albuterol Sulfate Inhalation Solution, 3 mL in 25-,
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