Meridian Medical Technologies a Pfizer Company recalls EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 265
Recalled May 10, 2017 · FDA recall D-0691-2017 · Meridian Medical Technologies a Pfizer
Hazard
Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication · FDA Class I
Units
92,544 2-pak (U.S.); 198,579 syringes (O.U.S.)
Sold at
Nationwide and Puerto Rico, Argentina, Austria, Australia, Belgium, Chile, Croatia, Czech Republic, Denmark, Estonia, Finland, France, Germany, Ireland, Italy, Japan, Latvia, Lithuania, Netherlands, New Zealand, Norway, Poland, Portugal, Romania, Saudi Arabia, Singapore, Slovakia, Slovenia, Sweden, Switzerland, Taiwan, Thailand, United Kingdom. There has been no U.S. government or military distribution.
Description
Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
Product
EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 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 Jr. 0.15 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.
Manufacturer(s)
Meridian Medical Technologies a Pfizer Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →