Aerosol products higher risk for benzene: scientist behind recalls
Dove, Nexxus and Suave are among recalled dry shampoo brands sold nationwide that may contain the human carcinogen.
Watch CBS News
Dove, Nexxus and Suave are among recalled dry shampoo brands sold nationwide that may contain the human carcinogen.
On Wednesday, the U.S. Food and Drug Administration (FDA) amended the emergency use authorizations of the Moderna and Pfizer COVID-19 bivalent vaccines to authorize their use as a single booster dose in younger age groups.
The Food and Drug Administration is warning pet owners about a common chemotherapy drug that is possibly killing dogs.
The FDA cleared kid-size doses — just a third of the amount given to teens and adults — for emergency use, and up to 28 million more American children could be eligible as early as next week.
More than 200 million eggs distributed to restaurants and grocery stores in nine states have been recalled because of bacterial contamination.A notice posted on the Food & Drug Administration website Friday said the eggs shipped from a North Carolina farm may be tainted with salmonella. The bacteria can cause nausea, diarrhea and, in rare cases , death. Twenty-two illnesses have been reported.
The proposal would also require tanning bed users to sign consent forms acknowledging the risks of the radiation-emitting devices.
Stryker Interventional Spine announced the clearance of 510(k)s, United States Food and Drug Administration approval allowing the sale of two additional products in its portfolio.
The Allegan-based health and beauty products manufacturer Perrigo Co. (Nasdaq: PRGO) said Wednesday it has received final approval from the United States Food and Drug Administration for its abbreviated new drug application for morphine sulfate 100ml/5 percent oral solution.
Perrigo Co. announced that it has received final approval from the United States Food and Drug Administration for its abbreviated new drug application for calcium acetate capsules, the generic equivalent of Phoslo Gelcaps.
MichBio, the biosciences industry association in Michigan, announced today that it is visiting Capitol Hill Monday and Tuesday. The primary agenda item will be the pending User Fee reauthorizations -- Prescription Drug User Fee Act and Medical Device User Fee Act (MDUFA) -- as well as the new Generic Drug User Fee Act and Biologics and Interchangeable Products User Fee Act.
Ann Arbor-based Tangent Medical Tuesday announced submission of a United States Food and Drug Administration 510(k) application for its NovaCath Secure IV Catheter System, developed from extensive clinical research of health care worker and patient needs.
Perrigo Co. Tuesday announced it received Food and Drug Administration clearance to market and distribute infant formula that contains 100 percent partially hydrolyzed whey protein.
Food safety partners are launching a campaign to reduce food poisoning due to undercooked pre-prepared foods.
Allegan-based Perrigo Co. has received final approval from the United States Food and Drug Administration for its abbreviated new drug application for over-the-counter Minoxidil Foam, a generic version of Men's Rogaine Foam
The Food and Drug Administration wants to know if there could be a link between the artificial food coloring and hyperactivity in children.
Terumo Cardiovascular Systems, an Ann Arbor-based subsidiary of Terumo Corporation of Tokyo, Japan, announced it has agreed to the terms of a consent decree with the U.S. Food & Drug Administration regarding quality system improvements at the company's Ann Arbor plant.
The Food and Drug Administration said Friday it has received several reports of liver damage with Multaq tablets, including two cases in which patients had to have their livers removed.
Krunchers! Inc. are recalling all Jays Original Potato Chips because the bags don't show a milk allergen warning.
