Women in Canada filed a transvaginal mesh class-action lawsuit, which Boston Scientific has agreed to settle for $21.5 million. According to news reports, the proposed settlement involves about 325 women whose share of the settlement
Homestar North America has recalled 33,000 Finch 3-drawer dressers because they pose a tip-over hazard that poses a risk of serious injury, entrapment, or death for children. According to an alert issued by the US
A House Representatives committee is asking children’s products manufacturers Graco and Chicco to consider recalling their popular baby products citing dozens of infant deaths that have been linked to infant sleepers. According to a report
Deaths related to traumatic brain injuries from falls are increasing across the United States, according to a report released last week by the Centers for Disease Control and Prevention (CDC). Researchers used death certificate data
Researchers say disposable vapes are the hot item on school campuses and have replaced Juuls. An NPR news report suggests that efforts to curb teen vaping are slightly behind schedule. By the time Juul pulled most
Ikea is recalling 820,000 dressers, which are at risk of tipping over and crushing small children, adding to the 17.3 million dressers recalled by the furniture retail giant in 2016. According to USA Today news
Six women who received breast implants linked to a rare form of cancer are suing Allergan for failing to warn the public about the health risks posed by these implants. According to a report on
The Federal Motor Carrier Safety Administration (FMCSA) has launched a comprehensive study of the causes of large truck accidents with the intention of using that information and data to guide its enforcement priorities in the
Estimates of pedestrian fatalities from the Governors Highway Safety Association (GHSA) indicate that the upward trend continued through last year. According to news reports, in 2019, pedestrian deaths were up 5% compared to the previous year
Researchers with the U.S. Food and Drug Administration (FDA) who conducted a long-term study of women implanted with transvaginal mesh to treat pelvic organ prolapse (POP) concluded that the FDA should have banned the products
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