Latest Kaiser Health News Stories
The federal agency took 14 months to warn the public about the potential for infections. Officials say they acted as fast as they could.
Why an obscure revenue raiser for the Affordable Care Act has found its way into a number of congressional campaign ads.
The agency found several prominent facilities had not followed rules on reporting incidents in which patients were harmed.
The FDA confirms it is looking into more than one problem with the compressor, which is used to power patients’ artificial hearts.
High-intensity focused ultrasound, often not covered by insurance, leads to discussions about which patients benefit in the real world.
The drug’s manufacturer says it has an expiration date of 12 to 18 months but that includes distribution time, so many customers find they have to buy a new device at least once a year.
A closer look shows that industry lobbying was just one factor in EpiPen’s sales explosion.
In a small study, Minnesota researchers found that the infant drops used to increase visibility during procedures may create a “perfect habitat” for bacteria and make scopes harder to clean.
Two Los Angeles area patients alleged a prominent UCLA spine surgeon harmed them by using Medtronic devices in experimental ways without their consent and failing to disclose his financial ties to the company. Both UCLA and Medtronic deny wrongdoing.
U.S. Rep. Ted Lieu (D-Calif.) renews his call for tightened laws that would force manufacturers to notify the Food and Drug Administration when they issue safety warnings in other countries related to the design and cleaning of their devices.
Newly released court documents show that after Tokyo-based Olympus Corp. alerted customers in Europe in 2013, it told its U.S. operation not to warn U.S. doctors and hospitals. Since then, at least 35 patients have died after being sickened in outbreaks.
After a wave of sometimes-deadly superbug infections, the agency last year ordered a recall of Custom Ultrasonics machines used to disinfect medical scopes. Now, with little explanation, it is backing off.
House panel concludes inquiry on superbug outbreaks; one member prepares legislation “to make sure these situations don’t happen again.”
The device manufacturer had a close relationship with Ronald Reagan UCLA Medical Center in Los Angeles — until its scopes were linked to infections and the company raised the price for new ones by 28 percent.
The company will pay $646 million to end civil and criminal probes. Olympus’ leaders acknowledge responsibility for ‘past conduct’ they say was inconsistent with the firm’s values.
Why is a 200-year-old icon of the medical field still in wide use in the digital age? Some say modern tools are more informative and worth the extra cost, but the stethoscope has staunch defenders.
The medical device industry is enjoying a two-year moratorium on a tax that was created to support the Affordable Care Act. Are firms using their savings to create more jobs, as many claim?
In a respected medical journal, a specialist advises colleagues on protecting patients but doesn’t mention potential infections from a contaminated scope at his Philadelphia cancer center.
Despite dozens of infections from medical scopes, an agreement on how to fix the FDA’s flawed regulation of the device industry remains elusive.