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FDA proposes asbestos-testing standards for talc products

FDA proposes new tests to detect asbestos in cosmetics and other products containing talc

The proposed rule is required under a law passed by Congress last year, and is intended to ensure the safety of makeup and baby powder.

UPI · 1d

FDA proposes rule to target asbestos in talc cosmetic products

The U.S. Food and Drug Administration (FDA) has proposed a new rule to require standardized testing of talc-containing cosmetics for asbestos, a known carcinogen linked to serious illnesses.

CNN on MSN · 1d

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 recalls eye drops

ABC · 18h

Systane eye drops recalled due to fungal contamination: FDA

One lot of Systane Lubricant Eye Drops Ultra PF, manufactured by Alcon Laboratories, has been recalled due to fungal contamination, the FDA announced this week.

Yahoo · 1d

Over-the-counter eye drops sold in Hawaii recalled due to fungal contamination

The Hawaii Department of Health is notifying residents of a recall issued by Alcon Laboratories for their over-the-counter eye drops.

Irish Star on MSN · 21h

Eye drops recalled nationwide for risk of ‘fungal contamination’ that can cause eye infections

The US Food and Drug Administration has recalled Systane Lubricant Eye Drops Ultra PF due to a risk of fungal contamination. The eye drops are typically used to cause temporary relief from dry eyes or irritation.

Bristol Myers Squibb, FDA and Opdivo

Reuters · 23h

FDA approves injectable version of Bristol Myers Squibb's cancer drug Opdivo

The U.S. Food and Drug Administration said on Friday that it has approved an injectable version of Bristol Myers Squibb's blockbuster cancer drug, Opdivo.

Yahoo · 23h

US FDA approves injectable form of Bristol Myers' Opdivo

The U.S. Food and Drug Administration said on Friday that it has approved an injectable version of Bristol Myers Squibb's blockbuster cancer drug, Opdivo. (Reporting by Sneha S K and Sriparna Roy in Bengaluru;

Newsable Asianet News on MSN · 18h

Bristol Myers Squibb Stock In Focus After FDA Approves Cancer Drug: Retail Sentiment Brightens

Shares of Bristol Myers Squibb ($BMY) were in the spotlight on Friday after the U.S. Food and Drug Administration approved an injectable version of the pharmaceutical major’s cancer drug Opdivo. Opdivo is reportedly part of PD-1 inhibitors class of drugs,

FDA raises recall alert to highest level

Hosted on MSN · 12h

Prebiotic Supplement Recall in 25 States As FDA Issues Risk Warning

Customers who purchased the supplement are advised to discontinue use immediately and inspect their product to identify if it matches the recalled batches.

NBC News on MSN · 1d

Recalled Costco eggs may cause severe illness due to salmonella, FDA warns in new alert

Federal food regulators raised their alarm for recalled eggs sold from Costco stores over possible salmonella exposure, reclassifying the targeted product to its highest risk level.

Yahoo · 13h

Costco egg recall may cause 'serious' illness or death, FDA says as it raises risk level

The recall is now Class I, meaning that "there is a reasonable probability that use of the product will cause serious, adverse health consequences or death," according to the Food Safety and Inspection Service,

Newsweek on MSN35m

Cocktail Recall Update As FDA Issues Risk Warning for 25 States

A bartender serves Bloody Mary cocktails at an event in New York City. A Bloody Mary cocktail mix recall has been classified as Class II by the FDA. A bartender serves Bloody Mary cocktails at an ...

2don MSN

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.

Scientific American18h

The FDA Is Changing What Foods Can Be Called ‘Healthy’

Whole grains and fruits are in, and added sugar is out. That’s going to change what’s on a lot of cereal boxes and other things ...

Everyday Health17h

FDA Approves First Medication for Obstructive Sleep Apnea

By aiding weight loss, Zepbound can improve symptoms of obstructive sleep apnea (OSA) in people with obesity — but CPAP ...

3don 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 ...

Hosted on MSN2d

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 ...

1don 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 ...

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FDA proposes asbestos-testing standards for talc products

FDA recalls eye drops

Bristol Myers Squibb, FDA and Opdivo

FDA raises recall alert to highest level

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