After checking the over-the-counter drugs using a low-heat method of testing, the FDA said it found much lower levels of NDMA than was discovered with a higher temperature test employed by Valisure.

UK medicines watchdog the Medicines and Healthcare Products Regulatory Agency (MHRA) slapped an alert on one batch of Zaditen 0.25mg/ml eye drops, used to treat seasonal allergies such as hay fever.

GlaxoSmithKline on Tuesday said it is recalling the popular heartburn medicine Zantac in all markets as a "precaution", days after the U.S. Food and Drug Administration found "unacceptable" levels ...

The MHRA described the recall as Class 2, which means the defect may cause mistreatment or harm to the patient but is not life-threatening or serious. It applies to two batches of pills.

An analysis of global usage patterns of a common hypertension drug following a major recall demonstrates the worldwide impact of contamination at a single manufacturing facility. The research, led by ...

The MHRA described the recall as Class 2, which means the defect may cause mistreatment or harm to the patient but is not life-threatening or serious. Chemists have been told: "Stop supplying the ...

More than 7,700 packs that have already been distributed are subject to the recall, according to the MHRA. People with the wrongly-labelled medication are being urged to contact their GP or ...

Patients have been told that the common drugs were dispensed with prescription Comments News Ben Hurst 13:21, 09 Jun 2025Updated 13:52, 09 Jun 2025 An urgent recall has been issued for batches of ...