U.S. Food and Drug Administration

Updated at 11:16 p.m. ET

The Food and Drug Administration is cautioning the public about the reliability of a widely used rapid test for the coronavirus. The test, made by Abbott Laboratories, has been linked with inaccurate results that could falsely reassure patients that they are not infected with the virus.

The Trump administration has promoted the test as a key factor in controlling the epidemic in the U.S., and it's used for daily testing at the White House.

States are beginning to receive cases of an experimental COVID-19 drug that the Food and Drug Administration authorized for emergency use on May 1.

But the distribution process so far has puzzled some hospitals and states about why they've been left empty-handed.

Updated at 4:59 p.m. ET

The Food and Drug Administration has given emergency use authorization to the antiviral drug remdesivir to treat hospitalized patients with the coronavirus, President Trump on Friday told reporters at the White House.

Gilead CEO Daniel O'Day said remdesivir maker Gilead Sciences is donating 1.5 million vials of the drug and will work with the federal government to distribute it to patients in need.

The U.S. Food and Drug Administration has approved a new system developed by Columbus-based Battelle to sterilize up to 160 thousand surgical masks a day amid the COVID-19 pandemic. 

Sandwiches sold in Ohio are being recalled because of concerns over possible Listeria contamination.  

Updated 6:14 p.m. ET

The Trump administration announced it will crack down on certain vaping products containing fruit, mint and other e-cigarette flavors to keep them away from kids. Manufacturers will have 30 days to take these products off the market before the Food and Drug Administration can take enforcement action.

Fuji Food Products Incorporated is issuing a voluntary recall of its ready-to-eat sushi, salads, and spring roll products sold in central Ohio over concerns of possible Listeria contamination.  

The Trump administration's plan to ban most flavored vaping products has stalled out, at least for the moment.

Two months ago, President Trump announced he was pursuing the new policy to put a dent in the youth vaping epidemic. The plan was supposed to have been unveiled in a matter of weeks.

But industry pushback and the politics of vaping appear to have derailed that process.

When President Obama signed the Family Smoking Prevention and Tobacco Control Act in 2009, it gave government regulators an important new weapon in its battle against Big Tobacco.

For the first time, the Food and Drug Administration had the power to regulate the manufacturing, distribution and marketing of tobacco products, including the new and then-largely unknown practice of vaping.

The Food and Drug Administration sent a letter to the food industry on Thursday, urging companies to get behind the initiative to standardize the use of the phrase "best if used by" on packaged food labels.

The U.S. Food and Drug Administration just approved one of the most sought after vaccines in recent decades. It's the world's first vaccine to prevent dengue fever — a disease so painful that its nickname is "breakbone fever."

The vaccine, called Dengvaxia, is aimed at helping children in Puerto Rico and other U.S. territories where dengue is a problem.

An Indiana-based company has issued a recall for melon products sold in Ohio and 15 other states after being linked to a salmonella outbreak. 

A state appeals court has cleared online retailer Amazon of wrongdoing in the death of an Ohio teen.  

Records obtained by the Associated Press show the state did not hesitate to spend the first round of federal funding targeting the opioid crisis, unlike other states, to expand Medicaid. 

The Food and Drug Administration announced a set of major new enforcement actions Wednesday aimed at reducing the sales and marketing of electronic cigarettes to teenagers.

Saying vaping among teenagers has reached "an epidemic proportion," the agency said it was taking a "series of critical and historic" measures to curb the alarming trends.

Federal health officials say they've confirmed more than 500 cases of people who became sick with an intestinal illness after eating McDonald's salads. 

Editor's note: Story updated with additional information about generic pricing on August 17.

The Food and Drug Administration has approved the first identical alternative to the EpiPen, which is widely used to save children and adults suffering from dangerous allergic reactions.

The FDA Thursday authorized Teva Pharmaceuticals USA to sell generic versions of the EpiPen and EpiPen Jr for adults and children who weigh more than 33 pounds.

The Food and Drug Administration says it has again found listeria in the production kitchen of Columbus-based Jeni's Splendid Ice Creams.

The U.S. Food and Drug Administration has approved a new label for a common abortion-inducing drug that could undo restrictions on medication abortions passed by Ohio and other states.

Listeria in packaged salad produced at the Dole plant in Springfield is being blamed for killing one person and sickening several others.

Some of the Dole Fresh Vegetables bagged spinach that has tested positive for salmonella was processed at a company plant in Springfield.

With two dozen scheduled executions in limbo, Ohio has sent a forceful letter to Washington asserting that the state can obtain a lethal injection drug from overseas without violating any laws. 

The U.S. Food and Drug Administration says the state would be breaking the law if it carried out plans to import lethal injection drugs.

A U.S. Food and Drug Administration probe of Columbus-based Jeni's Splendid Ice Creams says there was inadequate testing and cleaning in its local plant before listeria was found in some of its ice cream.