US Drug Recall Register
Class III · Low risk Terminated Initiated Nov 25, 2019 (7 years ago)

VCF Vaginal Contraceptive Foam, a) can, 13 applications per can, Net wt. 0.6 oz (17g)…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Defective Delivery System: canister unit exhibiting propellant leakage or loss, rendering the product and canister unusable

What was recalled

VCF Vaginal Contraceptive Foam, a) can, 13 applications per can, Net wt. 0.6 oz (17g). NDC 52925-312-14, b) case pack with 36 cans in a nested container. Net wt 0.6 oz (17g) per can. NDC 52925-312-06, Distributed By: Apothecus Pharmaceutical Corp. Oyster Bay, NY 11771.

Recalling firm
Apothecus Pharmaceutical Corp.
NDC code
52925-312-14
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0623-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.