Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg Recalled by Meridian Medical Technologies a Pfizer Company Due to Defective Delivery System; reports of the device failing...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Meridian Medical Technologies a Pfizer Company directly.
Affected Products
EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company; NDC 49502-500-02 ---- ALSO LABELED OUTSIDE THE US AS ---- Epipen Auto-Injector 0.3 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.
Quantity: 373,960 2-paks (U.S.) ; 331,738 auto-injectors (O.U.S.)
Why Was This Recalled?
Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Meridian Medical Technologies a Pfizer Company
Meridian Medical Technologies a Pfizer Company has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report