Personal Injury Attorney | Orlando Accident & Injury Blog
Defective metal-on-metal artificial hip implants are rapidly becoming the largest medical implant failure in years. The failure rate of these implants, the tens of thousands of patients who will need to have these implants surgically replaced, the costs of replacement and the scale of litigation involved all make this a very serious situation for taxpayers, who may be on the hook for billions in the coming years. Orlando personal injury lawyer James O. Cunningham has been following this story closely, as many people in Central Florida have had these devices surgically implanted in recent years before government investigations led to massive recalls of these implants.
On September 29, the U.S. Consumer Product Safety Commission (CPSC) issued a recall for around 2,300 drop-side cribs in the United States, and Health Canada has recalled another 800 in Canada. The recall affects drop-side cribs made by Sherman Inc. due to risks of entrapment, suffocation and fall hazards. The CPSC advises anyone who owns one of these cribs to stop using it immediately as the drop-side rail hardware used in construction of the cribs can break or fail, allowing the drop-side to become detached from the crib. If this occurs, a dangerous gap is created between the drop-side and the mattress, potentially trapping and hurting or suffocating an infant.
A 32-year-old Holly Hill man is facing murder charges after a 14-year-old boy died from a methadone overdose after finding the drug in the trash. The Volusia County State Attorney’s Office recently issued an indictment for the man for first-degree murder and a felony charge of delivering a controlled substance to a minor in connection with the boy’s death. The man is accused of driving the victim and another 17-year-old minor to Whitney Labs near Ormond Beach on Highway 1 early on the morning of May 24 and showing the boys how to find methadone the company has discarded in a dumpster.
Public Citizen, a national consumer advocacy group, is urging the Food and Drug Administration to issue a recall for a surgical product designed to help women with a common condition called pelvic organ prolapse. The FDA issued a warning about the product in July, and Public Citizen urges stronger action because the mesh device exposes patients to serious health risks and “the potential for permanent life-altering harm.” On average, around 300,000 women have surgery to correct pelvic organ prolapse, which happens when the muscles holding the bladder, bowel and uterus in place are weakened or stretched and these organs drop into the vagina.