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Over 140,000 bottles of generic Atorvastatin are recalled due to potential ineffectiveness, with no serious injuries reported.
Over 140,000 bottles of generic Atorvastatin Calcium Tablets, a common cholesterol medication, are being recalled due to failed dissolution testing, which may reduce the drug’s effectiveness.
The recall, classified as Class II by the FDA, involves 90-, 500-, and 1,000-count bottles with expiration dates from June 2026 to February 2027.
Manufactured by Alkem Laboratories in India and distributed by Ascend Laboratories in New Jersey, the medication is a generic version of Lipitor used to lower cholesterol and reduce heart disease risk.
No serious adverse events have been reported, but the FDA warns the drug may not work as intended.
Consumers are urged to check their lot numbers and consult a healthcare provider for guidance.
Más de 140.000 botellas de Atorvastatina genérica han sido retiradas del mercado debido a su potencial ineficacia, sin que se hayan reportado lesiones graves.