VCF Vaginal Contraceptive Foam — Class III drug recall D-0623-2020
Terminated recall by Apothecus Pharmaceutical Corp., reported 2019-12-25, distributed nationwide. Defective Delivery System: canister unit exhibiting propellant leakage or loss, rendering the product and cani
| Recall number | D-0623-2020 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Apothecus Pharmaceutical Corp., Hicksville, NY, United States |
| Recall initiated | 2019-11-25 |
| Classified | 2019-12-19 |
| Reported by FDA | 2019-12-25 |
| Terminated | 2024-09-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Reason classes | packaging |
| NDC | 52925-0312-06, 52925-0312-14 |
| Lot numbers | 31560, 31561 |
| Expiration dates | 2021-06 |
Product
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.
Reason for recall
Defective Delivery System: canister unit exhibiting propellant leakage or loss, rendering the product and canister unusable
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0623-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.