Florida Product Liability Attorneys
According to data recently made public by the US Food and Drug Administration (FDA), recalls of pharmaceutical drugs have surged in recent years, with 2014 shaping up to be the biggest recall year on record.
Orlando product liability lawyer James O. Cunningham would like to alert readers to an important product recall of frozen food that if ingested could cause serious health problems, especially for infants and the elderly. Buona Vita, Inc., a company based in Bridgeton, N.J., has announced that they are recalling nearly 73,000 pounds of frozen, ready-to-eat food products due to the potential contamination of the products with Listeria monocytogenes, a bacterium associated with food borne illness.
House of Raeford has announced that they are voluntarily recalling more than 4,100 pounds of a cooked chicken breast product due to possible bacterial contamination. After conducting an investigation, the U.S. Department of Agriculture’s Food Safety and Inspection Service said that the chicken may be contaminated with Listeria monocytogenes, which can lead to listeriosis, a potentially fatal disease. The product was distributed to delicatessens and food service facilities in Florida, Georgia, North Carolina and South Carolina for further processing.
In another news item that will come as no surprise to Florida residents or Orlando personal injury attorney James O. Cunningham, the federal government reports that it has received a surge of complaints in recent months about failed hip replacement devices. Researchers are still studying the dangers of some models of artificial hip devices, particularly metal-on-metal types, but early indications suggest persistent and very serious health consequences in association with faulty artificial hips. The Food and Drug Administration has reportedly received more than 5,000 complaints about metal-on-metal hips since January, more than the FDA has received about hip devices in the previous four years combined.
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.