FDA recall record

Norgestimate and Ethinyl Estradiol Tablets, USP, 0.18 mg/0.025 mg, 0.215 mg/0.025 mg, and recall — FDA D-0007-2026

Failed Content Uniformity Specifications

Class IIclassification
D-0007-2026official record ID
Oct 15, 2025report date

Recall record at a glance

Official recordD-0007-2026
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmAvKARE
Report dateOct 15, 2025
Recall initiation dateSep 2, 2025
Quantity2192 cartons
LocationPulaski, TN, United States

Official product description

Norgestimate and Ethinyl Estradiol Tablets, USP, 0.18 mg/0.025 mg, 0.215 mg/0.025 mg, and 0.25 mg/0.025 mg, 3 Units, 3x28 tablets blister cards per carton, Rx only, Manufactured for AvKARE, Pulaski, TN 38478. Carton NDC: 42291-565-84; Blister NDC: 42291-565-28

Why the product was recalled

Failed Content Uniformity Specifications

Distribution information

U.S. Nationwide

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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