FDA DrugClass IINotable
FDA Recall: Alyacen 7/7/7, Norethindrone and Ethinyl Estradiol Tablets USP, 0.5mg/0.035mg, 0.75mg/0.035mg, 1 mg/
Description
Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities.
Hazard
Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities.
Related Recalls
2026-06-24 · FDA_DRUG
FDA Recall: Burkhart topical anesthetic gel, benzocaine 20 %, Strawberry Flavor, 1 oz (30 mL), Manufactured for
Keystone Industries
2026-06-24 · FDA_DRUG
FDA Recall: Dental City TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, Strawberry Flavor, 1 OZ (30 g), Distributed by
Keystone Industries
2026-06-24 · FDA_DRUG
FDA Recall: Aripiprazole Tablets USP, Rx only, 30 mg, 30 tablets, Marketed by: Ajanta Pharma USA Inc., Bridgewat
Ajanta Pharma USA Inc
2026-06-24 · FDA_DRUG
FDA Recall: PureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavor, Manufactured for
Keystone Industries