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Medication Safety Alerts

Auvi Q Voluntary Recall


On October 28, 2015, Sanofi issued a voluntary recall of all Auvi-Q® injection 0.15 mg and 0.30 mg. This recall was issued because these products may not deliver the correct amount of medicine. If someone having a serious allergic reaction did not receive the intended dose, there could be serious health risks, including death.

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

You should not continue to use product that is affected by this recall. Please call your doctor right away for advice if you may have used affected product. Your doctor is familiar with your medical history and can suggest the best treatment option for you. Please call your doctor right away to obtain a prescription for an alternate epinephrine auto-injector.

CVS/caremark Response: If you currently have any unused Auvi-Q 0.15 mg or 0.30 mg, please call a Customer Care representative toll-free at 1-866-823-5184. We will give you more information and help with arrangements for the return of any affected product.

If you are currently using Auvi-Q Injection and have questions, Sanofi is directing people to call 1-866-726-6340 or visit You may also call the United States Food and Drug Administration (FDA) consumer inquiry line toll-free at 1‑888‑INFO-FDA (1‑888-463-6332) or visit their web site at

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