FDA recall record

VCF CONTRACEPTIVE PRE-FILLED APPLICATORS VCF, Vaginal Contraceptive Gel, Birth Control, 10 recall — FDA D-0151-2025

CGMP deviations: out of specifications for assay

Class IIclassification
D-0151-2025official record ID
Dec 25, 2024report date

Recall record at a glance

Official recordD-0151-2025
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmApothecus Pharmaceutical Corp.
Report dateDec 25, 2024
Recall initiation dateNov 22, 2024
Quantity33,659 retail boxes in US
LocationHicksville, NY, United States

Official product description

VCF, Vaginal Contraceptive Gel, Birth Control, 10 Pre-filled Applicators, Net Wt. 0.09 oz (2.55g) Each, Distributed By: Apothecus Pharmaceutical Corp., Ronkonkoma, NY 11779, NDC 52925-512-10

Why the product was recalled

CGMP deviations: out of specifications for assay

Distribution information

Nationwide in the USA and 2 Distributors in Hong Kong

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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