Sanofi US is voluntarily recalling ALL Auvi Q® (epinephrine injection, USP). The recall involves ALL Auvi Q currently on the market and includes both the 0.15 mg and 0.3 mg strengths. The Lot numbers include every consecutive lot number beginning with 2299596 through 3037230. The products have been found to potentially have inaccurate dosage delivery.
Patients who use Auvi-Q should call The Children’s Medical Group at 845.452.1700 for an alternate epinephrine auto-injector.
They only should use Auvi-Q in the case of a life-threatening allergic reaction in which no other injector is immediately available and then call 911, the alert said.