US Drug Recall Register
Class III · Low risk Terminated Initiated Dec 7, 2012 (14 years ago)

Bronkaid Dual Action Formula, Ephedrine Sulfate 25 mg/Bronchodilator, Guaifenesin 400…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Labeling: Label lacks warning or Rx legend; Certain information was inadvertently excluded from the product carton label.

What was recalled

Bronkaid Dual Action Formula, Ephedrine Sulfate 25 mg/Bronchodilator, Guaifenesin 400 mg/Expectorant, a) 24 coated caplets per blister pack, UPC 300240537879, b) 60 coated caplets per blister pack, UPC 300240537855, Bayer HealthCare LLC, Consumer Care, P.O. Box 1910, Morristown, NJ, 07962.

Recalling firm
Bayer Healthcare, LLC
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-177-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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