On October 1, 2017 a lone gunman opened fire from a hotel room overlooking a country music outdoor concert in Las Vegas with an estimated 22,000 people in attendance. The shooting began Sunday at approximately 10 p.m. local time. The shots led to a stampede as the panicked crowd ran for cover amid what has now been identified as the deadliest mass shooting in modern United States history, reports USA TODAY.
Country music singer Jason Aldean, the festival’s headliner was on stage when the rain of bullets began and continued to play through the first extended volley when the crowd became confused, unsure of what the sound was. The music stopped at about the same time the volley did, but after several moments, another, lengthy round of gunfire started, setting off chaos in the crowd. Social media videos show people ducking for cover and fleeing amid the unrelenting barrage of bullets.
When the music event, was interrupted by the gunfire, victims fell bleeding, concertgoers screamed, ran for cover, or did whatever they could to get away. “Get down,” one shouted. “Stay down,” screamed another.
The gunman, retired accountant Stephen Craig Paddock, 64, enjoyed playing high-stakes poker and was an avid gambler. It appears he killed himself shortly before police officers stormed the 32nd floor room he had rented at the Mandalay Bay Resort and Casino, according to Clark County Sheriff Joe Lombardo.
Investigators say that Paddock’s shooting rampage was painstakingly planned and included specially modified weapons and surveillance cameras designed to spy on any police intruders who might try and stop his murderous barrage.
Parker Waichman LLP is a national law firm available and prepared to assist anyone who has suffered personal injury, property damage, or death due to the gun violence at the Mandalay Bay Resort and Casino.
Paddock’s Weapon Collection
Authorities seized more than 40 firearms that Paddock had either at his home in Mesquite, Nevada, or in his hotel room. Police also seized thousands of rounds of ammunitions along with explosives.
Sheriff Lombardo described Paddock as the son of a 1960s bank robber on the FBI’s most-wanted list after escaping from prison, as “as a distraught person intent on causing mass casualties.” Lombardo felt Paddock was likely a “lone wolf” and that a motive for the shooting spree had not yet been determined, reports USA TODAY.
Las Vegas Mayor Carolyn Goodman said, “This is a crazed lunatic full of hate. This has been a hugely traumatic time for all of us.”
Paddock had checked into the Mandalay Bay on September 28, but it was still unclear whether he specifically requested the towering room, or how Paddock was able transport almost two dozen weapons into his room without it seeming suspicious. Granted, golf club bags, and other sport-equipment paraphernalia may go unnoticed. Sheriff Lombardo reported Paddock brought at least ten suitcases “over a period of time” into his hotel room.
Jill Schneider, Bureau of Alcohol, Tobacco and Firearms Special Agent, said Paddock had nearly 50 guns – a combination of rifles, shotguns and pistols – found in three locations. Authorities said Paddock increased the attack’s deadliness by adding more lethal components to his weapons. He had devices attached to 12 semiautomatic rifles that created a sound mimicking fully automatic gunfire.
Paddock’s brother, Eric Paddock, of Orlando, Florida, says his wealthy brother was a big spender at casinos and was often given free rooms and meals there. The brother told NBC News that he was “dumbfounded” by the shooting. “He was just a guy. He lives in Mesquite, he went to the hotels, he gambled, he went to shows…. We are completely at a loss.”
Video of the actual shooting captured nine seconds of continuous rapid fire, and then 37 seconds of silence from the weapon, but with panicked screaming from the crowd. Gunfire began again in at least two more bursts, both shorter than the initial assault, according to The New York Times.
Country singer Jake Owen, was on the stage with Mr. Aldean when the gunshots began. Owen told CNN that it was like “shooting fish in a barrel from where he was.”
In the first hours, 90 patients arrived at Sunrise Hospital and Medical Center, which was in walking distance of the concert. By noon on Monday, the next day, the Level Two trauma center was treating 180 victims.
Of those, 124 “met the criteria for trauma activation,” said Dr. Jeff Murawsky the hospital’s chief medical officer. Injuries included single and multiple gunshot wounds to the head, face, chest, body, arms and, in one, case a finger, The Times reports.
Legal Help for Gun Violence Victims
If you or someone you know suffered injury, emotional distress, property damage, or death at the Mandalay Bay Resort and Casino, you may be eligible for valuable compensation. Parker Waichman offers free, no-obligation case evaluations. We urge you to contact us at 1-800-YOURLAWYER (1-800-968-7529).
from Parker Waichman http://www.yourlawyer.com/blog/least-59-dead-500-wounded-las-vegas-mass-shooting/
Abbott Laboratories is being sued over allegations that St. Jude Medical, the Minnesota-based medical device company owned by Abbott, neglected to warn the public and regulators for years that thousands of its defibrillators contained faulty lithium batteries.
The federal lawsuit was filed in northern Illinois on September 18, alleging that St. Jude knew more than 250,000 implantable defibrillators it sold in the United States between 2011 and October 2016 had batteries that could suddenly short out and cause the vitally important devices to lose power with little or no warning. Abbott bought St. Jude three months after the recall, so was therefore responsible for the litigation, reports the Star Tribune.
Lawsuit Seeks Class-Action Status
The lawsuit is seeking class-action status to represent all self-insured and commercial insurance companies and estimates that those insurers collectively paid hundreds of millions of dollars for St. Jude Medical defibrillators. The suit seeks punitive damages as well.
Product liability attorneys at Parker Waichman LLP are actively reviewing potential lawsuits regarding allegedly defective medical devices including St. Jude defibrillators.
Formerly, St. Jude officials have defended their decision to wait until October 2016 to recall hundreds of thousands of the implantable defibrillators, saying executives and medical advisors worked as fast as possible to confirm the rare but serious problem.
The federal lawsuit makes ten claims that include failure to warn about known defects, breach of warranty, negligence, and unjust enrichment. The federal case also includes a claim that St. Jude officials violated Minnesota’s Prevention of Consumer Fraud Act when they “deceptively omitted” long-known facts about the device batteries until last October, the Star Tribune reports.
“If defendants had not omitted … or misrepresented the defects in the recalled devices, physicians would not have used the recalled devices,” the lawsuit says. “Accordingly, plaintiff and the other nationwide class members would not have incurred costs for the recalled devices and the medical costs of device removal and replacement surgery and other related costs.”
Premature Battery Depletion Leads to Deaths
St. Jude received 42 reports, the lawsuit says, showing evidence of premature battery depletion related to the lithium issue between 2011 and 2014. In 2014, St. Jude received a report that the problem had led to a patient’s death. The problem was documented in a journal article in December 2014.
St. Jude Medical made a change to its battery design on May 23, 2015, according to a Star Tribune report, in response to a problem that the company said it identified in 2014. However, the company continued selling the defibrillators that contained the old batteries until early October 2016.
This alludes to the fact that some patients received recall notices just weeks or months following surgery for a problem that St. Jude was aware of for years. St. Jude officials said they did not consider the change in battery design in 2015 to be an acknowledgment that they were aware at the time that the old devices were faulty, but rather, they felt they were taking a device that was performing well and improving on it. The decision to recall the devices in 2016 occurred only after enough cases of lithium battery defects were confirmed internally.
The 2015 design change was approved by the U.S. Food and Drug Administration (FDA). The FDA did not call for an immediate recall as the rate of problems at the time seemed low and was consistent with rates of problems with other issues in other models on the market. The increased rate of premature battery depletions was realized only later, leading to the recall.
The most recent data available was as of May 31, where 616 of the 398,740 affected defibrillators sold worldwide had depleted batteries with no other discernible cause than lithium shorting, St. Jude’s data showed. Two patients died when their defibrillators lost the ability to shock their heart back into a normal rhythm, reports the Star Tribune.
Controversy Over Immediate Device Replacement
Some doctors have remarked they would consider immediate device replacements for patients who are dependent on their defibrillators to also act as pacemakers to keep their hearts beating properly.
Not all affected devices are to be removed from patients, St. Jude’s voluntary recall announced in October. It recommends that patients consult with their doctors and use bedside remote-monitoring devices that analyze remaining battery life.
Affected recall devices include Fortify, Fortify Assura, Quadra Assura, Unify, Unify Assura and Unify Quadra implantable defibrillators made before May 2015, according to the Star Tribune.
However, St. Jude and the FDA do not recommend “prophylactic” replacement of all recalled devices as the replacement surgery has its own risks of potentially serious complications. An October 11 FDA safety communication said, “The rate of complications following replacement surgery are higher than those associated with premature depletion.”
“However, the FDA and St. Jude Medical recognize the need to weigh individual clinical considerations. If the decision is made to replace an affected device based on individual patient circumstances, St. Jude Medical has announced they will provide a replacement device at no cost.”
Have You Been Injured by a St. Jude Defibrillator?
If you or someone you know has sustained injury associated with a defibrillator, you may be eligible for valuable compensation. Parker Waichman personal injury law firm offers free, no-obligation case evaluations. We urge you to contact us at 1-800-YOURLAWYER (1-800-968-7529).
On September 15, Sig Sauer arms maker announced that some Sig 716 DMR, 516 Carbon Fiber and M400 Predators with two-stage triggers may have an incorrectly heat-treated hammer. “Over time this could result in a trigger malfunction creating a significant safety hazard,” a release from the company said. The statement was to notify the mandatory recall on certain models to replace the hammer and trigger assembly, reports Guns.com
The New Hampshire-based arms manufacturer notes that potentially affected models will have a “SIG” mark etched into the hammer and has a serial number look-up tool online with instructions to follow, to determine if a particular model is subject to the recall. Sig Sauer will correct any of the affected firearms at no cost to the customer. according to ammoland.com.
This recall does not affect any law enforcement or military rifles or any SIG, MCX, or MPX products.
Sig Sauer Inc. makes a variety of products to “meet any mission parameter,” including handguns, rifles, ammunition, electro-optics, suppressors, and ASP (Advanced Sport Pellet) airguns.
National law firm Parker Waichman LLP has extensive and successful experience in all kinds of litigation, including defective firearms. Attorneys at the firm are available to answer questions for individuals seeking legal information for potential lawsuits.
Previous Sig Sauer Problem
In August 2017, a Connecticut police officer filed a multimillion-dollar lawsuit against Sig Sauer for injuries he sustained when his department-issued P320 – a version of U.S. Army’s new service pistol – accidentally discharged when he dropped it and wounded him in the leg. Shortly after the incident, Sig Sauer issued a statement that it offered a voluntary upgrade to address unintentional discharges. The gun manufacturer said, the Army’s Modular Handgun System (MHS) is not affected by the upgrade, reports Business Insider.
“As a result of input from law enforcement, government and military customers, SIG has developed a number of enhancements in function, reliability, and overall safety including drop performance. SIG SAUER is offering these enhancements to its customers.”
Multiple Surgeries due to Accidental Shot Fired
The upgrade announcement came days after the officer filed the August 4 complaint in the U.S. District Court for the District of Connecticut. The officer had been loading equipment into the back of his car in January when he dropped his holstered P320. The gun accidentally fired when it hit the pavement. The 9mm bullet struck him under his left knee, and lodged to the side “with the round protruding from his leg,” according to the firearmsblog.com.
The officer is a 34-year-old member of the Stamford, Connecticut Police Department Special Response Team. He had to undergo multiple surgeries but is back on light duty. The lawsuit may require Sig Sauer to pay the officer more than $3 million in punitive and compensatory damages.
The fact that the gun went off unintentionally when the trigger had not been pulled, is very serious and the amount in damages sought reflects that.
The three counts include violation of the Connecticut Product Liability Act; violation of the Connecticut Unfair Trade Practices Act; and a Connecticut common law tort, which is negligent infliction of emotional distress. The officer is also demanding Sig Sauer recall the pistol or include a warning that the gun is not drop safe when a round, or bullet, is in the chamber, Business Insider reports.
Sig Sauer Responds
Sig Sauer claims in its statement that the P320 meets “U.S. standards for safety, including the American National Standards Institute (ANSI)/Sporting Arms Ammunition Manufacturers’ Institute Inc. (SAAMI); National Institute of Justice (NIJ); as well as rigorous testing protocols for global military and law enforcement agencies.”
The gun manufacturer, however, concedes, that “recent events indicate that dropping the P320 beyond U.S. standards for safety may cause an unintentional discharge,” the statement said. The Stamford Police Department said it has shelved all P320s it issued to its officers because of the incident.
In July, the leadership at Glock Inc. stated publicly that the Army’s decision to choose Sig Sauer to make its new MHS was driven by cost savings, not performance.
The Government Accountability Office denied Glock’s protest of the Army’s MHS decision, which Glock officials maintain was the result of “incomplete testing” and Sig Sauer’s $102 million lower bid.
The officer’s case may be settled out of court, but there is a possibility it could go to a jury trial. It was noted that the accidental discharge from the gun could have killed the officer, or shot a bystander, so the incident was taken very seriously, according to Business Insider.
Legal Information Concerning Potential Lawsuits
If you or someone you know has been injured by a defective firearm, you may be eligible for valuable compensation. Parker Waichman offers free, no-obligation case evaluations. We urge you to contact the attorneys at 1-800-YOURLAWYER (1-800-968-7529).
from Parker Waichman http://www.yourlawyer.com/blog/safety-warning-recall-notice-sig-sauer-rifles/
Breast implant-associated anaplastic large-cell lymphoma (ALCL) is a rare type of cancer that develops around breast implants. Australian health officials reported 56 cases of ALCL, including three deaths since 2007. The U.S. Food and Drug Administration (FDA) has reported eight deaths and more than 359 cases in the United States of ALCL in women with breast implants, reports the Daily Hornet.
Textured breasts implants, were more likely to cause cancer than smooth-surfaced breast implants, warns the FDA. Australian researchers published a study recently estimating that textured breast implants were 14 times more likely to cause ALCL than implants that are smooth-surfaced. In Australia, 90 percent of women with breast implants have textured-surface implants.
Textured Breast Implants are More Prone to Cause Cancer
Another study in Australia in 2014, revealed that textured breast implants were more likely to develop a bacterial coating called “biofilm.” This may cause low-level inflammation and immune system reactions that may cause lymphoma to develop in the fluid surrounding the implant.
Textured implants, which are treated with chemicals that etch the pouch surface, were introduced in the early 1990s. This was approximately five years before the first report of implant lymphoma. Texturing keeps the device firmly in place because scar tissue grows into the rough surface.
ALCL is a cancer that grows rapidly and it can be deadly if not treated. Symptoms include fever, fatigue, loss of appetite, night sweats, weight loss, and swollen lymph nodes in the neck, armpit, or groin, according to the Daily Hornet.
National law firm Parker Waichman LLP has extensive experience representing clients in all kinds of litigation. Our lawyers are available to answer questions for anyone seeking legal information about filing a lawsuit.
ALCL Case Histories
A Southern California woman decided to have a breast augmentation in 2000 and opted to get silicone pouches filled with saline. She considered this a safe choice, but in 2011, she experienced a “stabbing pain” in her left breast, which had ballooned because of swelling around the implant. She was diagnosed with a new type of lymphoma – a cancer of the immune system = caused by implants. The malignancy is distinct from breast cancer and very rare.
The FDA had first warned of a link in 2011. The lymphoma has been connected to both saline and gel implants, for enlargement as well as for reconstruction after breast cancer. Most patients in these cases had textured rather than smooth implants.
Since implants were introduced in the 1960s, for the first time, medical authorities, including the World Health Organization (WHO), agree that the prosthetics give rise to a disease in susceptible women. Some experts believe the controversial theory that implants can trigger debilitating autoimmune illnesses such as lupus, scleroderma, and fibromyalgia, as many women have contended since the 1990s, according to the Inquirer.
Robert Miranda, a pathologist at MD Anderson Cancer Center in Texas said, “To me that has to be evaluated again.” The Cancer Center has treated approximately 40 women with implant-related lymphoma.
The first recognized implant-related case of lymphoma was in California in 1997. By 2010, after a few dozen more case reports, Miranda and some other researchers noted it was a new disease entity: a rare blood cell malignancy, with even rarer genetic hallmarks, that developed around breast implants
In late 2016, the National Comprehensive Cancer Network, based in Fort Washington, issued diagnosis and treatment guidelines. Since the lymphoma is typically not aggressive, it can usually be treated by removing the implant, fluid, and the capsule of scar tissue that naturally forms around the prosthetic, the Inquirer reports.
However, the cancer can become life-threatening, as a woman from Ontario, Canada found out. She had no symptoms until the day after her first mammogram at age 50 in 2015. Her results were normal, but she felt lumps under an armpit. Her physician assumed the mammogram had ruptured her six-year-old textured gel implants. Ultimately, an MRI and biopsy revealed lymphoma that had spread to her bowel and lymph nodes.
Following two chemotherapy regimens that failed, doctors estimated the woman had six months left to live. A newer, targeted Hodgkin’s lymphoma drug saved her, but she still had to undergo a risky stem cell transplant as well as chest radiation.
Through her ordeal, she has become an activist. The woman founded a Facebook group for implant lymphoma patients, made a YouTube video, and recently met with the FDA about improving patient information, the Inquirer wrote.
“We want women to have objective, seamless information,” she said. “Implants are described as FDA approved. The truth is, implants were conditionally approved in 2006, and as of today, these conditions have not been met.”
Legal Information and Advice for Women
If you or someone you know has developed an illness as a result of a breast implant, you may have valuable legal rights. Parker Waichman LLP personal injury lawyers offer free, no-obligation case evaluations. We urge you to contact our attorneys at 1-800-YOURLAWYER (1-800-968-7529).
A new study published in Vaccine on September 13 is causing some concern for pregnant women who have received the flu vaccine or are considering it. The study of pregnancies in the United States found that women who had miscarriages between 2010 and 2012 were more likely to have had back-to-back annual flu shots that included protections against the H1N1 virus (swine flu).
The Centers for Disease Control and Prevention (CDC) has reached out to a doctor’s group, the American Congress of Obstetricians and Gynecologists, to warn them the study is coming out and help them prepare for a potential wave of worry from expectant mothers, CDC officials said.
Increased Incidence After Repeat Vaccine
“We are not saying this is a causal relationship,” said James Donahue, DVM, PhD, MPH, a senior epidemiologist at the Marshfield Clinic in Wisconsin and the lead author of the study, meaning the data does not necessarily show that the flu vaccine causes miscarriages. “There’s no biological basis for this phenomenon, so the study represents something that wasn’t expected.”
The study was conducted over two flu seasons (2010 to 2012), and involved 485 women. These women who experienced spontaneous abortion, or miscarriage, were matched with those who delivered full-term or stillbirths. Donahue and fellow researchers were examining if miscarriages were more apt to occur if a woman received the flu vaccine in the 28 days prior to the spontaneous abortions. The case-control study was funded by the CDC, according to CIDRAP (Center for Infectious Disease and Research Policy) News.
It was found by researchers that no association between miscarriage and flu vaccine appeared if a woman had not received a vaccine in the previous year, but in women who had consecutively gotten a flu vaccine containing the 2009 H1N1 virus, the investigators found an adjusted odds ratio (aOR) of 7.7. The women not vaccinated in the previous season had an aOR of 1.3. This increased association was seen in both seasons studies.
In the 28-day window, the overall aOR was 2.0, or double the risk, however those findings, in contrast to the H1N1 subset, were not statistically significant. There was no visible association in any other exposure window, reports CIDRAP News.
National law firm Parker Waichman LLP has extensive experience and success representing clients in all kinds of litigation. Lawyers at the firm are available to answer any questions you may have about pursuing a case.
Previous Studies Involving Flu Vaccine and Miscarriage
“In a previous study conducted on flu vaccine and miscarriage, we did not see a risk,” Donahue said, referring to research done from 2005 to 2007. That study was performed after the CDC made the recommendation 2004 that all pregnant women in all trimesters get the seasonal flu shot. After the 2009 H1N1 pandemic, the CDC requested a follow-up study.
“We can speculate that what we see here is vaccination with H1N1pdmo9 for the first time is like getting primed, then boosted,” said Donahue. “But now H1N1 is just a circulating seasonal virus; most children and young adults have been exposed by infection or vaccination.” In other words, there may have been a real effect in the seasons on the heels of the 2009 pandemic, however, further study will fail to show this association. Donahue and his co-workers are planning a follow-up study that examines more recent flu seasons and triples the number of cases, reports CIDRAP News.
Further Investigation Necessary
A research professor of global health at George Washington University, Lone Simonsen, PhD, said the timing of the study is of interest. She has done her own research showing that in 1918, when the world had another H1N1 pandemic that was worse than in 2009, the number of women who miscarried were as many as one in ten.
“In this case getting the flu vaccine can be like being introduced to a virus that was evolutionarily quite similar to the virus from 1918, she told CIDRAP News.
However, she also said the new study included only women with documented miscarriage. “Who are the women that document a miscarriage at 5 weeks?” asked Simonsen. “Probably someone who is also likely to get a flu shot.” If this is true, that may throw off numbers showing an association.
In an accompanying commentary in the same journal, three United States experts not taking part in the study said that miscarriage is one of the hardest birth outcomes to study in observational research.
“Among other factors, the high proportion of [spontaneous] abortions [SAbs] that take place in clinically-unrecognized pregnancies and the lack of consistency in accurate capture of these events in medical records when SAbs do occur, make such research difficult to carry out,” they write. After pointing out what they see as limitations of the study, and the implausibility of the prime-boost hypothesis, the experts write, “One important take-away message from this study is that seasonal vaccine formulations are not all the same.”
Both Donahue and Edward Belongia, M.D., the director of the Center for Clinical Epidemiology & Population Health at the Marshfield Clinic and a study coauthor, said this study in no way suggests reversing or revising the CDC’s advisories relating to pregnant women and flu shots.
“It’s very well known that getting the flu is bad for pregnant women and bad for the baby, and we have a vast amount of safety data on the vaccine,” said Belongia.
Legal Information and Advice About Flu Shots
If you or someone you know has been negatively affected by a flu vaccination, you may have valuable legal rights. The personal injury attorneys at Parker Waichman offer free, no-obligation case evaluations. We urge you to contact us at 1-800-YOURLAWYER (1-800-968-7529).
Britax Child Safety is recalling over 207,000 rear-facing infant car seats because part of a clip can break and cause a choking hazard. Britax says in government documents that since February, three customers found broken chest clips in the mouths of children but no choking injuries were reported, according to the Daily Hornet.
The company traced the cause to customers putting pressure on the clips, which help to properly position the harness straps. Britax advises that customers can safely continue using the seats if they remove the chest clip or monitor a center tab for signs of breakage. Britax will notify owners and provide a new chest clip, reports the Seattle Times. Britax has set up a website for owners to determine whether their seats are being recalled and for additional information.
The following model numbers are affected, if they were manufactured between November 1, 2015, or after May 31, 2017:
B-Safe 35 & Travel Systems
E1A183F, E1A185M, E1A185P, E1A186R, E1A203F, E1A205M, E1A205P, E1A206X, E1A206Z, E1A207E, E9LU65V, E9LU66X, E9LU66Z, E9LU67D, E9LU67E, EXA185M, S02063600, S02063700, S03803400, S03803500, S03803700, S03803800, S03803900, S04144400, S04144500, S04144600, S04145000, S04402800, S04884200, S04884300, S04975600, S04978900, S05260200, S06020300, S06020400, S06020500, S06020600, S06020700, S06020800, S06020900, S06147100, S921800, E1A193F, E1A195M, E1A195P, E1A196X, E1A196Z, E9LV16R, E9LV17D, S04144700, S04144800, S04144900, S04183700, S04183800, S04437700, S04884400, S04884500, S06051400, S06051500, S06051600, S06051700, S06051800, E1A233F, E1A235M, E1A235P, E1A236X.
Warranty Replacement Part: S03421600
B-Safe 35 Elite & Travel Systems
E1A215T, E1A215U, E1A216P, E1A221Q, E1A225C, E1A225U, E1A226L, E9LS51Q, E9LS56C, E9LS56L, E9LS57F, E9LS57G, E9LS57H, EXA216L, S01298600, S02063800, S02063900, S02064000, S04281200, S04281300, S04628500, S06018800, S06020000, S06020200, S92370, E9LV21Q, E9LV26C, E9LV26L, E9LV27F, E9LV27G, E9LV2Q8, S01298700, S04184000, S06051300, E9LT15U, E9LT16C, E9LT16L.
BOB B-Safe 35 by Britax
E9LT34A, E9LT34C, E9LT35X, EXLT34A, E9LT54A, E9LT54C, E9LT55X
Britax reported that it began seeing an increase in warranty claims due to chest clip damage in October 2016, one year after the company changed the material it used to make the clips in response that they were too easily opened. “The chest clip is not a required safety device: it is added to the harness system to help position the shoulder straps,” the notice said.
National law firm Parker Waichman LLP has extensive experience and success in representing clients in product liability litigation. Our attorneys are actively reviewing cases on behalf of individuals who are seeking information for those interested in filing a potential lawsuit.
Prior Britax Car Seat Recall
In January 2016, Britax received reports of cracks developing around the carry handle on some infant car seats. This could allow the handle to break and a baby to be injured. This does not affect the crash-worthiness of the car seat. Do not use the carry until you have received and installed the repair kit. Affected car seats were manufactured between October 1, 2014, and July 1, 2015. For a complete list of B-Safe 35, B-Safe35 Elite, and B-Safe 35 Travel System model numbers affected, please visit the Britax website.
Car seat recalls are not very common, but on occasion, companies must recall car seats in order to better protect your baby. You should register your car seats with the manufacturer to receive the fastest notification of any applicable recalls. If your car seat is not yet registered, you can do so easily by calling the manufacturer (there should be a phone number right on one of the car seat labels) or visiting their website.
It is also recommended to check National Highway Safety and Traffic Administration’s (NHTSA’s) extensive recall list if you borrow a car seat from a friend or have to use an older car a seat again after a period of non-use.
Graco My Ride 65
On May 10, 2017, over 25,000 Graco My Ride 65 convertible car seats were recalled because the harness webbing may n adequately restrain a child in a crash. Graco will provide registered owners with a replacement harness.
Baby Trend Hybrid LX 3-in-1 Centennial
December 19, 2016, a small number of Baby Trend Centennial 3-in-1 boosters were recalled because the center adjuster rivet could pull through or break if it is used with a child that weighs more than 40 pounds.
Kiddy World Plus
Nearly 1,500 Kiddy World Plus combination car seats were recalled on April 29, 2016, because the buckle may only partially engage, and may not sufficiently protect a child in case of a crash.
Evenflo Transitions 3-in-1
Transition car seats manufactured before January 29, 2016, were recalled because a child could reach the center front harness adjuster and loosen the harness. This could allow a child to be improperly restrained, which might lead to injury in a crash. Evenflo provides a remedy kit to prevent a child from reaching the harness adjuster.
Information on Filing a Product Liability Lawsuit
If you or someone you know has been injured by a defective or recalled product, you may have valuable legal rights. Attorneys at Parker Waichman LLP offer free, no-obligation case evaluations. For more information contact us at 1-800-YOURLAWYER (1-800-968-7529).