December 6, 2002
Pharmacia Corporation Has Recalled
Lunelle Monthly Contraceptive Injection
The Food and Drug
Administration (FDA) has released the following information.
Lunelle Monthly Contraceptive Injection (medroxyprogesterone acetate 25mg
cypionate 5mg) Injectable Suspension, Single Use 0.5 mL syringe and
physician samples, For
Intramuscular Use Only, Rx only. Recall # D-064-3.
All lots distributed in 2002.
Recalling Firm: Pharmacia Corporation, Kalamazoo, MI, by press release on
October 10, 2002.
Manufacturer: Pharmacia Corporation, Puurs, Belgium.
Firm initiated recall is ongoing.
Subpotency; the active ingredients.
VOLUME OF PRODUCT IN COMMERCE