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Logan is an AV Rated Attorney who was born in Los Angeles, California and raised on a farm in Utah. At an early age, he learned the value of hard work by performing chores on a dairy farm and, together with his brothers, delivering the regional daily newspaper to subscribers in their hometown.
At 19, Logan served a two-year mission for the Church Of Jesus Christ of Latter-Day Saints in Italy where he learned to speak, write, and read Italian – an ability he still has today. He went on to earn a degree in Accounting at the University Of Utah in 1996 and received a Juris Doctor from the University Of Tulsa College of Law in 1999. He also earned a Masters Degree in Taxation from the University Of Tulsa College Of Business in 1999.
Professionally, Logan has worked in public accounting, as a Vendor Manager for a Fortune 100 company that specialized in drafting and managing supplier agreements, as a controller for a privately-owned telecommunications support company, and as the controller for a mid-size law firm.
Logan has experienced numerous successes in helping clients recover as individual plaintiffs, claimants and as litigants involved in prior and current matters such as:
In re: Prempro Products Product Liability Litigation, MDL 1507, alleged that use of hormone replacement therapy drugs, such as Prempro, drugs caused breast cancer.
In re: Accutane Products Liability, MDL 1626, use alleged to have resulted in bowel diseases, such as Ulcerative Colitis or Crohn’s Disease.
In re Mirapex Product Liability Litigation, MDL 1836, alleged use caused pathological gambling and other compulsive behaviors.
In re Chantix (Varenicline) Products Liability Litigation, MDL 2092, alleged use resulted in a wide variety of side effects and risks, including behavioral changes, depression, aggression, agitation, hostility, rage, suicidal ideation, suicide attempts, and suicide.
In re: Zicam Cold Remedy Marketing, Sales Practices and Products Liability Litigation, MDL 2096, alleged that use of Zicam nasal cold remedy products caused anosmia (the loss of sense of smell).
In re Yasmin and YAZ (Drospirenone) Marketing, Sales Practices and Products Liability Litigation, MDL 2100, alleged use resulted in various serious side effects, including deep vein thrombosis (DVT), pulmonary embolism (PE), and ischemic stroke (CVA).
In re: Zimmer Durom Hip Cup Products Liability Litigation, MDL 2158, complications alleged to have resulted from devices include premature implant loosening, metallosis, tissue damage, premature failure, and the need for early revision surgery.
In re: DePuy Orthopaedics, Inc., ASR Hip Implant Products Liability Litigation, MDL 2197, complications alleged to have resulted from devices include multiple revision surgeries and complications such as stroke, pulmonary embolism, deep-vein thrombosis, hip dislocation and foot drop (abnormal gait).
In re: Actos (Pioglitazone) Products Liability Litigation, MDL 2299, alleged that individuals who use Actos face an increased risk of developing bladder cancer.
In Re: Skechers Toning Shoe Products Liability Litigation, MDL 2308, products are alleged to have caused serious injuries, including broken feet and ankles, leg and hip fractures, tendon and ligament damage, head injuries, and spinal cord damage.
In Re: National Football League Players’ Concussion Injury Litigation, MDL 2323, former NFL players allege to have sustained head trauma resulting in long-term cognitive health problems while playing for the NFL and accuse the League of failing to inform them of the risks linked to concussions and neglecting to minimize brain injury risks to protect their short and long-term cognitive health
In Re: Mirena IUD Products Liability Litigation, MDL 2434 alleged that use led to uterine and internal organ perforation,
In Re: Incretin-Based Therapies Products Liability Litigation, MDL 2452, plaintiffs allege that the use of one or more of four anti-diabetic incretin-based medications – Janumet (sitagliptin combined with metformin), Januvia (sitagliptin), Byetta (exenatide) and Victoza (liraglutide) – caused them or their decedent to develop pancreatic cancer.
Individual plaintiff actions against Medtronic related to the use of the Medtronic Infuse Bone Growth, or Infuse BMP alleging risks such as unwanted bone growth (ectopic bone growth), inflammatory reactions, adverse back and leg pain events, radiculitis, retrograde ejaculation in men, urinary retention, bone resorption, and implant displacement.
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