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Alyacen 7/7/7, Norethindrone and Ethinyl Estradiol Tablets USP, 0.5mg/0.035mg, 0.75mg/0.035mg, 1 mg/0.0.35mg, 3 Blister Cards each containing 28 tablets, 28 day regimen, Rx only,…

Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities.

Class II Medicine & devices FDA June 24, 2026 Reached Texas
Read the official FDA notice →

What to do

Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.

Details

Recalling company
Glenmark Pharmaceuticals Inc., USA — Elmwood Park, NJ
Severity
Class II — moderate
Reported
June 24, 2026
Recall number
D-0588-2026
Status
Ongoing
Source
FDA

Where it went

USA Nationwide.

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