It seems like U.S healthcare is more concerned about profits than patients these days. Now is the time to learn more about the latest legal battles patients face with conditions from head to toe and how to be your own best healthcare advocate, so you receive the care you deserve.
On Nov. 4, I blogged about the Food & Drug Administration’s (FDA’s) public statement announcing the detection of N-nitrosodimethylamine (NDMA) in preliminary tests of the heartburn medication ranitidine, which is most often sold under the brand name Zantac. NDMA is a chemical agent categorized as…
On Oct. 19, the FDA announced J&J’s recall of nearly 33,000 bottles of its 22-oz Baby Powder. This came alongside a Johnson & Johnson (J&J) disclosure that a government test detected traces of cancer-causing asbestos particles in a sample of J&J Baby Powder. The recall…
On Sep. 13, the Food & Drug Administration (FDA) issued a public statement announcing that low levels of N-nitrosodimethylamine (NDMA) were detected in preliminary tests of the popular heartburn medication ranitidine, which is most often sold under the brand name Zantac. NDMA is a chemical…
Recently, I have been covering ongoing updates regarding the outbreak of e-cigarette or vaping product use-associated lung injury, or EVALI, as an alarming number of U.S. vape users fall ill. While the illness case count confirmed by the Centers for Disease Control (CDC) was just…
The Centers for Disease Control and Prevention’s (CDC) ongoing investigation of vaping-related lung disease is expanding by the day, with the number of reported cases and deaths rapidly rising in the U.S. In fact, there have now been 1,299 confirmed vaping-related lung disease cases and…
On Sep. 19, the Centers for Disease Control (CDC) announced the eighth U.S. death linked to vaping-related lung disease as a Missouri man in his forties. This came just four days after California’s Tulare County Health and Human Services Agency announced the seventh death on…
On Sep. 9, the U.S. Food and Drug Administration (FDA) issued a warning letter to JUUL Labs Inc., which dominates the U.S. e-cigarette market with their vaping products. According to the letter, JUUL has been engaging in illegal and deceitful marketing tactics by making unproven…
On Sep. 3, 2019 Sixteen (16) health, environmental, farmer, and farmworker organizations released a joint statement calling for the Environmental Protection Agency (EPA) to remove glyphosate from the U.S. marketplace due to an abundance of evidence linking it to a type of cancer called non-Hodgkin’s…
On Aug. 10, 2018, a California state jury unanimously found that Monsanto’s glyphosate-based Roundup weed killer caused plaintiff Dewayne “Lee” Johnson to develop a type of cancer called non-Hodgkin’s lymphoma (NHL). The jury also found that Monsanto failed to appropriately warn Roundup users of this…
Previously, I blogged about the Nov. 28, 2018 recall of Stryker’s Tritanium posterior lumbar (PL) cage. The cage was recalled after reports of cage fractures occurring during and after surgical implantation, putting patients at-risk for a number of medical complications. The surgical technique is being…
