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FDA Recalls Duloxetine Antidepressant for Cancer Risk

Cucumber Recall Update as FDA Gives Walmart Products Highest Risk Level

The recall of Marketside Fresh Cut Cucumber Slices from 34 Walmart stores in Texas has been given a Class I risk classification by the U.S. Food and Drug Administration (FDA). The classification was announced on Wednesday following the initial recall,

Yahoo · 3d

FDA Recalls Duloxetine Antidepressant for Cancer Risk: What to Know

Over 8 million U.S. adults take antidepressants to treat mild to moderate depression, anxiety and, in some cases, chronic pain. A recent Food and Drug Administration (FDA) recall of a commonly prescribed antidepressant,

Health on MSN · 2d

Duloxetine Recall: FDA Sets Second-Highest Risk Level for Antidepressants Containing Potential Carcinogen

Fact checked by Nick Blackmer Certain bottles and doses of duloxetine, a common antidepressant, have been recalled due to the presence of potentially cancer-causing chemicals.The recall was initiated on Nov.

Newsweek on MSN · 1d

Antidepressant Recall Update As FDA Sets Risk Level

233,003 bottles of duloxetine have been recalled due to potentially containing high levels of cancer-causing impurities.

FDA, Biden and nicotine

UPI News on MSN · 5h

FDA asks Biden administration to reduce nicotine content in tobacco products

The U.S. Food and Drug Administration has proposed a rule that would significantly lower the amount of nicotine in tobacco products.

CNN · 21h

In Biden administration’s final days, FDA advances proposal to set a nicotine limit on tobacco products

As the Biden administration winds down, the US Food and Drug Administration has submitted a proposed rule that could significantly lower the amount of nicotine in tobacco products and potentially prompt more people to quit smoking.

U.S. News & World Report · 8h

FDA Asks Biden Administration to Limit Nicotine in Tobacco Products

In what appears to be a last-ditch effort to limit the harms of smoking before its term ends, the Biden administration has proposed a rule that would significantly lower the amount of nicotine in tobacco products.

FDA considers ban on artificial food dyes

Food & Wine · 1d

The FDA May Finally Ban This Controversial Food Additive

Red No. 3 — is found in many American foods such as cereals, beverages, snacks, and candies. But it may soon be banned nationwide by the FDA. Here's what you need to know.

Fox News · 1d

FDA looks to ban red food dye

Celebrity fitness trainer Jillian Michaels joins ‘Hannity’ to discuss the possibility of the FDA banning red food dye.

Yahoo · 1d

FDA considering ban on red dye

United Airlines continues to bring joy to families who need it most during the holidays with a trip to the north pole and the FDA is considering a ban on red dye in foods. Jane King is at the Nasdaq with those stories.

Granola, FDA

Food & Wine · 1d

The FDA Just Issued a Massive Recall on Granola Bars Sold Nationwide

The FDA just announced a massive, nationwide recall on MadeGood granola bars in several flavors due to the "potential presence of a piece of metal in the product. Here's what you need to know.

Yahoo · 20h

FDA Announces a Nationwide Recall on Granola Bars Due to Potential Metal Contamination

MadeGood granola bars, due to the potential presence of metal pieces, which pose a safety hazard if consumed. According to MadeGood's website, the company disclosed, "There is a very small risk that some of our granola bar products made between January and November 2024 may contain a piece of metal.

Health on MSN · 1d

FDA Announces Major Recall of MadeGood Granola Bars—Check Your Pantry For These Products

Batches of MadeGood granola bars have been recalled over potential metal contamination.Several customers complained of small, flat brush bristles in the products, which can cause injury if consumed.MadeGood said to return the recalled granola bars,

MedPage Today4h

FDA Issues Safety Alert on Liver Disease Drug

Postmarketing data on obeticholic acid (Ocaliva) identified a risk for serious liver injury in primary biliary cholangitis ...

US FDA identifies cases of liver injury after treatment with Intercept's drug

Intercept Pharmaceuticals' liver disease drug is being observed for injury to the organ in patients without severe scarring, ...

thelundreport1h

The FDA hasn’t inspected this drug factory after 7 recalls for the same flaw, 1 potentially deadly

Indian drugmaker Glenmark Pharmaceuticals issued a string of recalls for pills that didn’t dissolve properly. In one case, ...

FierceBiotech6h

FDA expands use of J&J’s Impella heart pumps to pediatric patients

The FDA has opened up the use of Johnson & Johnson’s miniaturized heart pumps to certain pediatric patients, including ...

Salsa Recall as FDA Sets Risk Level

The Food and Drug Administration ( FDA) has set the risk level for a corn salsa at a "class 2 recall," stating that 192 jars ...

BioPharma Dive1d

GLP-1 drug compounding is in limbo. Will the FDA draw out its decision?

The agency is due to make a determination on the shortage status of Zepbound by Dec. 19. But another delay could be possible ...

4hon MSN

Who do Americans trust for health information? Poll finds gap between FDA and RFK Jr.

In the latest Axios-Ipsos poll, 66% of respondents said they have a great deal or fair amount of trust in health information ...

Food Processing6h

FDA Leaders Grilled by a Testy Senate Committee on Ultraprocessed Foods, Chemical Additives

In the waning days of both the Senate committee and FDA leaders, Commissioner Robert Califf and Deputy Commissioner Jim Jones ...

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FDA Recalls Duloxetine Antidepressant for Cancer Risk

FDA, Biden and nicotine

FDA considers ban on artificial food dyes

Granola, FDA

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