The increase in vaping-related illnesses – known as e-cigarette or vaping product use-associated lung injuries (EVALI) – prompted the FDA to officially ban flavored e-cigarette pods in January 2020. However, this move is only one step toward holding e-cigarette manufacturers like Juul accountable for a decade’s worth of questionable marketing practices.
According to the FDA, there are more than one million annual surgeries to correct a hernia and 90 percent of them use a mesh patch. Varying complications occur for nearly one-third of all patients, from localized pain to life-threatening bowel perforations, requiring repair or complete mesh removal.
Earlier this year, Johnson & Johnson voluntarily recalled its baby powder after FDA testing found traces of asbestos in a sample purchased online. In October, the pharmaceutical company released a statement claiming that 15 tests of the same sample the FDA examined, completed by third-party agencies, contained no asbestos.
Monsanto first introduced Roundup, a glyphosate-based herbicide, in 1974 as a solution for weed control. The innovative, less-toxic products were geared toward growing commercial crops, but also could be used by the at-home gardener. In the 1990s, the company capitalized on this need by adding a line of crop seeds for corn, soybeans and canola, immune to Roundup’s effects.
Cities with high numbers of opioid overdoses are suing drug manufacturers for downplaying the serious side effects of this drug class. On this subject, the Justice Department’s Inspector General released a critical assessment at the beginning of October 2019. The lengthy document indicates the Drug Enforcement Administration (DEA) did not step in as overdoses increased and painkillers flooded the black market. The Inspector General claims their practices, many with loopholes and insufficient monitoring, are partially to blame.