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FDA Proposes New Testing Rules
US FDA proposes standardized testing to detect asbestos in talc products
The U.S. Food and Drug Administration is proposing that cosmetic products containing talc should be tested using standardized methods to detect asbestos, a potential contaminant, according to documents posted on the federal register on Thursday.
FDA proposes new testing rules to ensure cosmetics are asbestos-free
The Food and Drug Administration is proposing a rule that cosmetic companies would have to take extra steps to ensure that any products containing talc are free of asbestos.
FDA Proposes Rule to Require Standardized Testing Methods for Detecting and Identifying Asbestos in Talc-Containing Cosmetic Products
Today, the U.S. Food and Drug Administration (FDA) announced a proposed rule to establish and require standardized testing methods to detect and identify asbestos in talc-containing cosmetic products.
FDA issues highest-level recall for Costco eggs
FDA escalates recall of Costco eggs to include risks of 'severe illness or death'
There were approximately 10,800 retail units of the affected eggs sold at 25 Costco stores in five states beginning on Nov. 22.
FDA elevates Costco's quarter-million egg recall to its highest risk level
The Food and Drug Administration (FDA) has issued a new warning about thousands of recalled eggs sold at Costco (COST) stores due to potential contamination with salmonella, a bacterium that can cause serious infections.
Costco eggs recalled in Tennessee over salmonella fears classified as highest risk level
The FDA classified a November recall over potential salmonella contamination for eggs sold at Costco at its highest risk level.
FDA recalls eye drops
FDA Announces Nationwide Eye Drops Recall Due to Fungal Contamination
Systane eye drops were recalled earlier this week after the company discovered a fungal contamination in one of its products.
Systane eye drops recalled for possible fungal contamination, FDA says
Systane brand eye drops were voluntarily recalled because of possible fungal contamination, the Food and Drug Administration said.
Potential 'fungal contamination' leads to nationwide recall of popular brand of eye drops: FDA
A popular brand of eye drops is being recalled nationwide after a consumer reported a "foreign material" was found in a sealed vial, causing potential contamination.
FDA, GLP-1 and Type 2 diabetes
FDA Approves Generic GLP-1 Medicine For Diabetes Treatment
THURSDAY, Dec. 26, (2024 HealthDay News) -- The U.S. Food and Drug Administration (FDA) announced on Monday the approval of the first generic version of a daily injectable GLP-1 medicine for people living with Type 2 diabetes.
FDA approves generic GLP-1 drug to treat type 2 diabetes
The U.S. Food and Drug Administration has approved the first generic version of Victoza (liraglutide injection), significantly improving access to diabetes
FDA rejects GLP-2 drug candidate
Zealand Pharma's GLP-2 drug candidate fails to gain FDA approval due to request for additional trial to confirm efficacy and safety.
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FDA Says Decongestant in Many Cold Medicines Doesn't Work. So What Does?
Changes are coming to the cold and cough aisle of your local pharmacy: U.S. officials are moving to phase out the leading ...
Staten Island Advance
14h
FDA to phase out decongestant found in over-the-counter medicines: It doesn’t work
“Based on our review of available data, and consistent with the advice of the advisory committee, we are taking this next step in the process,” said Patrizia Cavazzoni, M.D., director of the
FDA
’s ...
2d
on MSN
FDA approves first medication for obstructive sleep apnea, which also promotes weight loss
The FDA approved a new drug treatment for obstructive sleep apnea that improves the condition through weight loss. Sleep ...
14h
on MSN
Startup led by Seattle doctors gets FDA approval for virus-killing, surgical mask technology
Seattle's Singletto is ramping up sales of surgical masks treated with its virus-killing technology and exploring other ...
3d
on MSN
US FDA revokes authorization for four COVID antibody drugs
The U.S. Food and Drug Administration has revoked the emergency use authorization for four COVID-19 antibody-based drugs, ...
2d
on MSN
The shortage of popular weight loss drug tirzepatide is over, FDA says. Patients could see higher costs as a result.
The weight loss medication tirzepatide (Mounjaro and Zepbound) is no longer in shortage, according to the FDA. Access to ...
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