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Medication Safety Alerts

Mucinex® Fast-Max® Products Voluntary Recall

09/04/2015

On September 4, 2015, the United States Food and Drug Administration (FDA) issued a notice regarding a voluntary recall of various Mucinex® Fast-Max® products manufactured by Reckitt Benckiser. This recall was issued because the Drug Facts part of the label may be missing certain active ingredients and safety warnings.

This may represent a potential health hazard or safety risk to plan members who may be using product affected by this recall.

A complete list of the affected products and lot numbers is provided here:

Please call your doctor right away for advice if you may be using affected product or if you do not know if you used affected product or not. Your doctor is familiar with your medical history and can suggest the best treatment option for you. If you need a prescription for a different medicine, please call your doctor.

CVS/caremark Response:

Please note: These products are not carried by the CVS/caremark Mail Service Pharmacies.

If you are currently using Mucinex Fast-Max products and have questions regarding this recall, please call your doctor or call Reckitt Benckiser toll-free at 1-888-943-4215, 8:00 am to 8:00 pm (ET) or visit www.mucinex.com/recall. You may also call the FDA consumer inquiry line toll-free at 1‑888‑INFO-FDA (1‑888-463-6332) or visit their Web site at https://www.fda.gov/.

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