Pharmacy Services
Medroxyprogesterone Acetate & Estradiol Cypionate Injectable Suspension (Lunelle) - Product Recall
October 14, 2002
Pharmacia voluntarily recalled all lots of medroxyprogesterone acetate / estradiol cypionate prefilled syringes (Lunelle) due to possible subpotency and reduced efficacy. Product packaged in vials is not affected by this recall. Additional information is available at the following links:
- MedWatch Alert:
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm154507.htm - Letter to Pharmacists/Wholesalers:
http://www.fda.gov/downloads/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/UCM170927.pdf - Letter to Physicians:
http://www.fda.gov/downloads/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/UCM170925.pdf - FDA News Release:
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm170924.htm
Updated
October 14, 2002; University of Utah, Drug Information Service. Copyright 2009, Drug Information Service, University of Utah, Salt Lake City, UT.
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