Brandon Smith
Partner at Childers, Schlueter & Smith, LLC
I’m M. Brandon Smith, a partner at Childers, Schlueter & Smith in Atlanta, Georgia, helping injured people nationwide with pharmaceutical litigation, mass torts, product liability, and serious personal injury cases.
Posts
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Defective 3M Combat Earplug Lawsuits Continue, How To Seek Help
Military service members thought they were protecting themselves with 3M Dual-Ended Combat Arms Ear Plugs. Unfortunately, the devices offered no protection when worn as instructed by the company.
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Weight Loss Drug Belviq Pulled From Market Due to Potential Cancer Risk
Promising weight-loss drug Belviq has been pulled off the U.S. market due to the potential risk of cancer. At the request of the U.S. Food and Drug Administration (FDA), drug manufacturer Eisai Inc. has voluntarily withdrawn and discontinued sales of Belviq (lorcaserin). The FDA took…
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Attorney Ashley Spires Joins The CSS Family
Childers, Schlueter & Smith is pleased to announce Ashley Spires recently joined our team. Prior to joining the firm, Ashley was a partner with a National civil litigation defense firm where she successfully litigated and tried cases in defense of nurses, doctors, medical practices, product…
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Hernia Mesh Lawsuits Mounting, But Alternative Hernia Repair Options Remain Widely Unavailable
Though no longer trending at the top of the news, the devastating consequences of defective hernia mesh continue to impact thousands of people in the United States on a daily basis. Hernia mesh is the net-like medical sheet used in over one million hernia repairs…
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J&J Rushed Test Results for Asbestos in its Baby Powder
Recently, I blogged about Johnson & Johnson’s Oct. 18 recall of nearly 33,000 bottles of its baby powder, which came alongside a disclosure that a government-funded test detected traces of cancer-causing asbestos particles in a sample of the powder. The contaminated sample came from Baby…
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More Ranitidine (Zantac) Recalls Issued Over Possible Carcinogen NDMA
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…
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FDA Ordered Testing Finds Asbestos in Johnson & Johnson Talcum Baby Powder
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…
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Zantac Heartburn Medication Recalled After Detection of Cancer-causing Chemical NDMA
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…
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U.S. Teens Likely to Face Long-term Consequences of Vaping Addiction
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…
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EVALI: The Name CDC Clinicians Gave to Deadly Vaping-Related Lung Disease
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…
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