FDA Drug recall D-0623-2020
VCF Vaginal Contraceptive Foam, a) can, 13 applications per can, Net wt. 0.6 oz (17g)
- FDA Drug
- Class III
- terminated
- Published 2019-12-25
On 2019-12-25 the FDA classified a Class III recall of VCF Vaginal Contraceptive Foam, a) can, 13 applications per can, Net wt. 0.6 oz (17g) by Apothecus Pharmaceutical, citing defective Delivery System: canister unit exhibiting propellant leakage or loss, rendering the product and canister unusable.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0623-2020 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2019-11-25 |
| Published | 2019-12-25 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Apothecus Pharmaceutical |
| Distribution | US |
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
Defective Delivery System: canister unit exhibiting propellant leakage or loss, rendering the product and canister unusable
Identifiers
| code_info | Lot # 31560, 31561 exp. date 06/2021 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0623-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.