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Summer Infant Baby Bather Recall Lawsuit
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Summer Infant Baby Bather Recall Lawsuit
Summer Infant Baby Bather Recall Lawsuit
Summer Infant has recalled 2 million baby bathers sold under its two brands in the United States following consumer complaints of seat collapse, leading to fall injuries and skull fractures to infants. On August 20, 2012, the U.S. Consumer Product Safety Commission warned about fall hazard and reported injuries associated with these Chinese-made bath seats and asked the manufacturer to consider market withdrawal of these products. The recalled products include two of Summer Infant bather brands, Mother's Touch and Deluxe Baby Bathers, which were sold between September 2004 and November 2011.
Why Summer Infant Baby Bather Recall
According to the Consumer Product Safety Commission, faulty design of Mother's Touch and Deluxe baby bathers is the main reason for the accidental fall, causing injury to the child seated on it. These baby bathing seats, about 13.4 inches in length and 12.4 inches in width, are available with blue or pink plastic bases. The bathers have also a sling seat, a white wire frame, and five rivets holding adjustable side hinges. The folding wire frames in Mother's Touch and Deluxe brand baby bathing seats fold suddenly or detach from the side hing when lifted or carried, posing a fall hazard to the infants.
Manufacturer Summer Infants has received at least seven complaints of infant fall, resulting in five injuries. Four babies aged between two weeks and two months suffered skull fractures while the fifth one had head injuries, leading to emergency medical care.
The recall information on manufacturer’s website says this is a “corrective action program” and “voluntary recall to repair with free locking strap and instructions.”
Other Summer Infant Recalls
In February 2011, Summer Infant recalled 1.7 million baby video monitors following complaints of strangulation hazard caused by these products, which were manufactured in China and were being sold in the United States since 2003. The U.S. Consumer Product Safety Commission admitted of receiving at least seven reports of deaths of babies and toddlers caused by monitors. Probes into incidents revealed that children died after being strangled by monitor cords placed closed to them. In one case, a toddler found with cord of the monitor rolled around his neck.
The Consumer Product Safety Commission also issued recall of 58,000 Summer Infant monitors sold under another brand, Slim and Secure, for possible burn injuries. The rechargeable batteries in these monitors could overheat and burst putting parents, children, and property at the risk of burn hazards.
Stryker Rejuvenate Hip Recall
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Stryker Rejuvenate Hip Recall
Stryker Rejuvenate Hip Recall Modular Hip Replacement Implant Lawsuit
A personal injury lawsuit filed in the Bergen County superior court in the first week of August has sought compensation from Stryker Orthopedics alleging that its defective Rejuvenate hip-replacement parts have caused serious health problems. The plaintiff, a 66-year-old woman from Florida, underwent right hip replacement in October 2011. Within months, she felt acute pain and her blood samples were found to contain high metal level though the Stryker Rejuvenate modular hip implant was intact. In June 2012, she had a revision surgery to get rid of abnormal tissue growth close to her hip. The plaintiff had to undergo more surgeries after experiencing a number of complications, including fractures, associated with the metal modular hip implant.
On July 4, 2012, Stryker Orthopedics issued a nationwide recall of its Rejuvenate Modular metal hip implant stems along with another of its brand, ABG II neck stems. The orthopedic implant manufacturer cited the risk of “potential fretting and/or corrosion at or about the modular-neck junction, which may result in adverse local tissue reactions manifesting with pain and/or swelling” as the reason for its market recall.
Stryker Rejuvenate Hip Implant Hip Replacement System
Stryker leads the global market for hip implant components with a variety of femoral, acetabular, and restoration equipment used in artificial hip implants. Stryker Rejuvenate modular hip implant has three important parts, a titanium neck, a chromium-cobalt stem, and a ball made of non-metallic materials. Patients implanted with these metal hip components have been diagnosed with a sharp rise in chromium and cobalt levels in their blood. According to post-marketing data, as many as 60 complaints were filed with the FDA against complications caused by Stryker Rejuvenate modular hip implant components between January and July 2012.
Sexual Abuse Lawsuit Attorney
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Sexual Abuse Lawsuit
Sexual Abuse Lawsuit
Five more men have joined 22 others in filing sexual abuse claims against the Irish Christian Brothers at a Chicago bankruptcy court. The plaintiffs have alleged abuse by the members of the Catholic order during their student years at Chicago-based Brother Rice and Leo high schools and St. Laurence High School in Burbank. The Catholic order has filed for bankruptcy protection and Wednesday was the deadline for filing of claims by sexual abuse victims.
The claims filed by five men last week alleged molestation by Brother Edward Courtney, who worked as a teacher at Chicago area schools of the Irish Christian Brothers during the 1960s and 1970s. Courtney along with Brother D.P. Ryan and Brother Robert Brouillette has been named in a number of sexual abuse lawsuits filed in Washington, New York, and other states. The Catholic order reportedly transferred Courtney from one school to other following molestation allegations before he joined its schools in Washington.
In April 2011, the Irish Christian Brothers filed for Chapter 11 bankruptcy after more than a dozen sexual abuse lawsuits claiming molestation by its priests were filed in the United States. Attorneys view the bankruptcy plea as an attempt to protect the church assets and prevent escalation in sex abuse lawsuit. All members of three school alumni associations were informed of the Wednesday deadline to file their sex abuse claims.
Irish Christian Brothers Sexual Abuse Lawsuit
The officials of the Christian Bothers have been named in a number of sexual abuse lawsuits filed in Ireland, Canada, Australia, and the United States since the early 1990s. According to a report of the Irish Commission to Inquire into Child Abuse allegations published in 2009, “allegations of child abuse, and particularly child sexual abuse, were a recurring and persistent problem for the Congregation.” The investigation found that physical beating and emotional torture were commonly used in schools and orphanages run by the order, and the climate of fear created by such action of the officials deterred many victims of abuse to report their abusers. According to the report, seniors did not take any step to dismiss the abusers, but transferred them from school to school, allowing them to continue their misdeeds.
In January 2009, the Congregation of Christian Brothers paid $7 million to 13 former students of Kent-based Briscoe Memorial School to settle sexual abuse lawsuits filed by them. The men alleged physical and sexual abuse over decades during the 1960s and 1970s, when they were part of the boarding schools run by the Catholic order. In November 2010, the order settled sexual abuse lawsuits filed by another group of 11 men for $4.45 million. The plaintiffs accused officials of the Christian Brothers of molesting them while they were students at the school in 1950s. The Seattle Archdiocese, owner of the schools, also paid $2.7 million as compensation. Another molestation victim from 1940s batch at the school settled for $315,000 in 2007. In 2006, the order settled three lawsuits alleging sexual abuse at Briscoe.
Health Care Lawsuit The Obamacare Lawsuits Explained
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Health Care Lawsuit The Obamacare Lawsuits Explained
Court Rejects Obamacare Lawsuit Challenging Contraceptive Coverage Provision
On July 17, 2012, a Nebraska federal court dismissed a lawsuit filed by seven states challenging contraception coverage requirements in the federal health care law. Judge Warren Urbom of Lincoln tossed out the federal lawsuit on the ground that the plaintiffs did not have the standing to file a lawsuit seeking to block the part of the Patient Protection and Affordable Care Act (PPACA). The Republican-dominated administrations in seven states, Nebraska, Florida, South Carolina, Michigan, Texas, Ohio, Oklahoma, and Texas, along with co-plaintiffs, a nun, a missionary, and three Nebraska-based church-affiliated institutions, the Catholic Mutual Relief Society of America, Pius X High School, and Catholic Social Services had challenged the contraception rule on the ground that it was against their religious liberties.
The act, popularly known as Obamacare, is a brainchild of President Barack Obama and seeks to extend affordable health care benefits to all U.S. citizens. The President signed the bill into law on March 23, 2012, following a series of considerations by the Congress for over a year. The United States Supreme Court upheld the health care overhaul law on June 28, 2012.
The Health and Human Services mandate under the Affordability Care Act makes contraception coverage a part of all health care plans, including those for employees working in institutions affiliated to religious bodies. The Catholic Church that runs hospitals, schools, and outreach programs strongly opposes the use of birth control measures. These religious bodies argued before the court that the challenged part of the act was a violation of their rights to reject contraceptives and abortion-causing drugs for women.
Read more: Health Care Lawsuit The Obamacare Lawsuits Explained
Hip Replacement Recall Lawsuit Stryker Biomet Wright Smith Nephew Hip Implant Recall Lawsuit Attorney
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Hip Replacement Recall Lawsuit Stryker Biomet Wright Smith Nephew Hip Implant Recall Lawsuit Attorney
Stryker Rejuvenate Hip Recall Depuy Hip Replacement Implant Recall Lawsuit Attorney
Stryker Orthopaedics has announced a national recall of its Rejuvenate Modular and ABG II brands of neck stems used for metal hip implants. The Michigan-based orthopedic implant manufacturer has terminated the sale of the two modular-neck stems used for hip replacement surgeries following discovery of potential risks. According to the information on the Stryker website, the devices are found to have “potential fretting and/or corrosion at or about the modular-neck junction, which may result in adverse local tissue reactions manifesting with pain and/or swelling. and ” In June 2012, Stryker recalled Rejuvenate hip implants in Canada for similar reasons. With 16 percent share of global orthopedic market, Stryker manufacturers a number of primary acetabular, femoral, and restoration hip implant components. Hip replacement implant recall lawsuit attorneys have filed hip implant lawsuits against Depuy Hip , Stryker Hip , Smith And Nephew Hip , Wright Medical Hip , Biomet and Stryker.
The July 4 recall was prompted by more than 60 complaints of hip replacement failure, including 40 reports of injuries related to Rejuvenate modular-neck stem since January 2012, against Stryker hip implants filed with the FDA adverse impact reporting system. Post-marketing surveillance data shows the patients implanted with these hip neck-stem implants and metal on metal hip replacement implants such as the Depuy ASR are at increased risk of metallosis because of release of metal particles into human blood streams following corrosion and erosion of these devices. Design problems cause metal hip components in these neck stems to rub against each other leading to discharge of cobalt and chromium into the blood. The unacceptable level of corrosion also renders Rejuvenate Modular and ABG II hip implant neck stems ineffective and put patients at the enhanced risk of device failure, pseudotumor formation, tissue destruction, infection, and bone necrosis. As with other metal hip implant recalls , the depuy and biomet hip lawsuits also focus on the similar metal poison from these recalled hip implants.
Stryker , Depuy , Biomet , Smith & Nephew Hip Implant Replacement Recall Complaints and Warnings
Stryker introduced Rejuvenate Modular hip implants in February 2010 asserting that the new product would provide improved intraoperative efficiency and flexibility. The modular hip system was approved by the FDA through its 510(k) clearance program, which does not mandate any safety trials for products “substantially equivalent” to those already in the market. Stryker claimed that Rejuvenate Modular hip implants were similar to the Profemur to ease regulatory approval. The Wright Profemur has been subject to a number of attorney lawsuits, citing early failure and metallosis similar to the issues found in other metal hip implants and at the root of most hip implant recall lawsuits from a doctor and attorney perspective.
In November 2007, the FDA warned Stryker about poor and unsanitary conditions at its Mahwah manufacturing facility, New Jersey, following an inspection of the plant. The regulator had been receiving complaints about product failures and a range of associated health problems since 2005. The admonition letter held deficient conditions responsible for faulty Stryker hip implants. The inspection team also discovered contamination at the plant by Staphylococcus bacteria, which can cause staph infections.
In January 2008, Stryker recalled two of its hip implant components, Acetabular PSL Cup and Hemispherical Cups, marketed under the Trident brand. The recall was made following growing concerns of contamination of these hip implants by “manufacturing residuals” beyond the permissible standards.
In March 2009, the American Academy of Orthopedic Surgeons recommended against using Stryker Trident cup hip implants because of their squeaking problems.
Vaginal Mesh Lawsuit
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Vaginal / Pelvic Mesh Lawsuit
Vaginal / Pelvic Mesh Lawsuit Ethicon Gynecare Recall & Transvaginal Mesh Defects
On June 4, 2012, women health product manufacturer Ethicon, Inc., announced that it would pull out its widely used Gynecare vaginal mesh implants following complaints of serious, life-threatening injuries associated with these products. The recall by the Johnson & Johnson subsidiary included four types of Gynecare mesh implants, TVT Secur, Prolift Pelvic Floor Repair System, Proflit MTM Pelvic Floor Repair System, and Prosima Pelvic Floor Repair System, which are subject to approximately 1,000 lawsuits consolidated under the federal multi-district litigation in Charleston federal court of West Virginia and coordinated litigation at New Jersey state courts.
About 300,000 women in the United States have these trans vaginal mesh devices implanted for pelvic organ prolapse and stress urinary incontinence. The recall was imminent after a FDA health alert in June 2011 expressed concern over a high number of injuries and deaths caused by Gynecare mesh implant side effects and questioned the real benefit of implanting these devices compared to traditional surgeries to treat pelvic prolapsed. The FDA adverse reporting system has received hundreds of complaints of consistent vaginal pain, extrusions, inflammation, bleeding, and other severe and permanent side effects that repeated surgeries failed to cure.
Gynecare Vaginal / Pelvic Mesh Implants
Vaginal mesh implants were allowed for hernia repairs in the 1950s. The FDA approved
their use in prolapsed surgeries in 2002. However, there were reports of their off-label use by doctors in abdominal surgeries in the 1980s and in vaginal surgeries toward the end of the 1990s. The mesh devices, made of polypropylene plastic, are implanted through pelvic floor surgery to support organs, such as bladder, urethra, uterus, bowel, and top of the vagina, in the pelvis of women against any drop, fall, or prolapse caused by weakening of muscles following pregnancy and other problems. In 2004, vaginal mesh kits were introduced to streamline and standardize the implant procedures. On an average, about 75,000 U.S. women undergo vaginal mesh implants every year.
Ethicon’s Gynecare vaginal mesh implants have almost 70 percent of the market share in the United States. Gynecare TVT mesh implant was approved by the FDA in 1998. However, Johnson & Johnson started selling Gynecare Prolift in 2005 without FDA approval. The manufacturer introduced Gynecare TVT Secur, the first mini-sling procedure, in late 2006. The FDA cleared its Gynecare Prolift+M for transvaginal implant in 2008. According to an estimate by the FDA, about 100,000 vaginal mesh implant operations were performed in the United States in 2010 alone.
FDA Warnings and Side Effect Reports Leading to Vaginal / Pelvic Mesh Recall
Gynecare vaginal mesh implants have been blamed for a high number of serious health problems in users. The FDA has received more than 1,500 complaints in the past three years claiming complications associated with these mesh implants. The FDA has categorized vaginal mesh implants as "Class II" medical device that can cause intermediate risk of harm in patients using it.
In 2008, the federal drug regulator notified the public about potential serious complications in patients caused by vaginal mesh implants. It listed urinary problem, pain, infection, and bladder perforations as key side effects of these products. The MedWatch alert also reported prolapse recurrence in patients implanted with these devices, which required additional surgeries.
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