FDA warns of problems with sterilization device
AP - 1 hour 9 minutes agoDoctors and hospitals should stop using a device from Steris Corp. to sterilize surgical tools after reports of malfunction, according to the Food and Drug Administration.
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Doctors and hospitals should stop using a device from Steris Corp. to sterilize surgical tools after reports of malfunction, according to the Food and Drug Administration.
Clinical research company Icon PLC said Friday it received a warning from the Food and Drug Administration about its management of two studies between 2004 and 2006.
Consumer products maker Unilever announced a recall of all Slim-Fast ready-to-drink products in cans due to possible bacterial contamination.
Pharmaceutical executives laid out plans Friday to prevent the misuse of prescription painkillers, under pressure from regulators trying to stop hundreds of fatal overdoses each year.
U.S. drug reviewers recommended that regulators further study the effects in children of a group of medicines known as atypical antipsychotics, a report released on Friday said.
Watson Pharmaceuticals Inc. said Friday it is challenging Takeda Pharmaceutical Co.'s patent on the insomnia treatment Rozerem.
Police in central Pennsylvania say a prankster who scaled a 400-foot radio tower to hang a bedsheet from an antenna needs to see a doctor right away.
Vitamin sales in the United States are expect to grow 8 percent this year to $9.2 billion, according to Nutrition Business Journal,.
Medical device maker St. Jude Medical Inc. said Friday the Food and Drug Administration approved a new neurostimulation device aimed at treating pain.
WASHINGTON -(Dow Jones)- Food and Drug Administration medical reviewers said Friday the agency should conduct an additional review of antipsychotic drugs to look at the impact of weight gain in children, a common side effect of the drugs.
Pharmaceutical Makers Presenting FDA with Risk Management Plans to Help Prevent Misuse of Prescription Painkillers
The U.S. Food and Drug Administration is recalling all Slim-Fast ready to drink products in cans because of possible bacillus cereus contamination. The micro-organism could cause diarrhea, nausea, and vomiting.
An economist at the Office of Management and Budget who has battled environmentalists for years on issues such as climate change and smog has raised questions about the economic impact of a proposed new rule on air pollution, according to documents obtained by The Washington Post.
The FDA lifted a clinical hold on CytRx's molecular chaperone candidate arimoclomol.
THURSDAY, Dec. 3 (HealthDay News) -- Kalbitor (ecallantide) has been approved by the U.S. Food and Drug Administration to treat dangerous flares of sudden fluid buildup in people with hereditary angiodema (HAE), the agency said.
Despite the FDA's recent rejection of experimental drug Ampligen, Hemispherx's CEO remains optimistic.