Recent changes
GovPing tracks this category across sources from 104 outlets, representing a portion of the 2,344 sources on GovPing, covering guidance, enforcement, rule, notice, and consultation instruments. In the past 7 days, 608 changes have been recorded.
Recent urgent actions include FDA's Class I recall of Draeger Atlan A350 anesthesia workstations for potential piston ventilator failure and a Good Brain Tonic recall after botulism contamination was identified. Health Canada also issued a Revolution Ascend CT recall for a security vulnerability, and FDA pulled Morovan nail polish remover (4,000 units) for prohibited methylene chloride.
Lockout Supplements Recalls Chocolate Syrup for Undeclared Sildenafil
Lockout Supplements is voluntarily recalling all lots of Boner Bears Chocolate Syrup nationwide due to undeclared sildenafil. The undeclared ingredient poses a risk of dangerous blood pressure reduction when interacting with prescribed medications.
EMA Recommends Six New Medicines for Approval
The European Medicines Agency's CHMP has recommended six new medicines for marketing authorisation and nine for extension of therapeutic indications. These recommendations cover treatments for various conditions including menopausal symptoms, liver disease, a rare genetic disorder, influenza, and graft-versus-host disease.
EMA Recommends Kygevvi for Rare TK2d Disease Treatment
The European Medicines Agency (EMA) has recommended granting a marketing authorisation for Kygevvi, a new treatment for the rare genetic disease thymidine kinase 2 deficiency (TK2d). This recommendation is based on clinical study data showing improvement in motor function for pediatric patients.
EMA Recommends Withdrawal of Levamisole Medicines
The European Medicines Agency (EMA) recommends the withdrawal of marketing authorisations for medicines containing levamisole due to the serious side effect of leukoencephalopathy. This recommendation follows an EU-wide review concluding that the benefits of these medicines no longer outweigh their risks for treating parasitic worm infections.
Levamisole withdrawn from EU market due to leukoencephalopathy risk
The EMA's PRAC has recommended the withdrawal of marketing authorisations for all medicines containing levamisole from the EU market. This decision is due to the confirmed risk of leukoencephalopathy, a serious brain side effect, where the benefits of the medicine no longer outweigh the risks for treating parasitic worm infections.
CVMP Opinions and Guidelines Update
The EMA's Committee for Veterinary Medicinal Products (CVMP) adopted positive opinions for several variations to existing veterinary medicinal products and discussed pharmacovigilance signals. These updates primarily involve product information changes based on signal management processes.
MHRA Raids Illegal Weight Loss Medicine Facility
The MHRA has raided two facilities suspected of manufacturing and selling illegal weight loss medicines, seizing nearly 2,000 doses and manufacturing equipment. This action is part of an ongoing investigation into a criminal network and aims to protect the public from dangerous, unregulated products.
Measles Exposure Alert at Denver Airport and Littleton Church
Colorado health officials have issued an alert for potential measles exposures at Denver International Airport and a Littleton church on February 21-22, 2026. The alert follows a confirmed measles case in an unvaccinated traveler. Public health agencies are offering free vaccinations to potentially exposed individuals.
MHRA Alert: Fake Mounjaro (tirzepatide) KwikPens
The MHRA has issued a notice regarding fake Mounjaro (tirzepatide) 15mg KwikPens dispensed by The Private Pharmacy Clinic in Birmingham. Patients with affected pens are advised to stop use immediately and report to the MHRA. The manufacturer reported five faulty pens.
MHRA Approves Imlunestrant Tosylate for Breast Cancer
The MHRA has approved imlunestrant tosylate (Inluriyo), a new treatment for adult patients with a specific type of advanced or metastatic breast cancer. This approval provides a new therapeutic option for patients who have not responded to prior hormonal treatment.
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616 changes in last 7 days
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104 official sources tracked
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