fda news - Search News

FDA recalls eye drops

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.

Fox Business on MSN · 2d

Potential 'fungal contamination' leads to nationwide recall of popular brand of eye drops: FDA

Irish Star on MSN · 1d

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.

FDA proposes asbestos-testing standards for talc products

CBS News on MSN · 1d

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, Opdivo and Bristol Myers Squibb

Reuters · 1d

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.

Business Insider · 14h

Bristol-Myers Squibb : FDA Approves Opdivo Qvantig For Subcutaneous Use In Adult Solid Tumors

Bristol Myers Squibb (BMY) announced Friday that the U.S. Food and Drug Administration has approved Opdivo Qvantig (nivolumab and

Seeking Alpha on MSN · 23h

Bristol-Myers gets FDA okay for injectable Opdivo

The FDA has reportedly approved an injectable formulation of Bristol-Myers Squibb's (NYSE:BMY) oncology drug Opdivo. Previously, the PD-1 inhibitor drug was only available through IV infusion. The injectable formulation,

FDA raises recall alert to highest level

Hosted on MSN · 15h

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 · 2d

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 · 16h

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,

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.

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 ...

Scientific American21h

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 Health20h

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 ...

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 ...

2don 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 ...

Some results have been hidden because they may be inaccessible to you

Show inaccessible results

FDA recalls eye drops

FDA proposes asbestos-testing standards for talc products

FDA, Opdivo and Bristol Myers Squibb

FDA raises recall alert to highest level

Related topics