Oct 15, 2021 · December 5, 2021 Update: As more victims look to file an NEC lawsuit against infant formula manufacturers, the maker of Similac (Abbott Laboratories) is now defending a related consumer class-action lawsuit alleging it made false and misleading comparisons between Similac Pro Advance and breast milk. Plaintiffs filed this new necrotizing enterocolitis …
Do I have a Baby Formula Lawsuit? The Schmidt Firm, PLLC is currently accepting baby formula induced injury cases in all 50 states. If your baby was born preterm or prematurely and developed Necrotizing Enterocolitis (NEC) after being fed baby formula in the NICU, you should contact our lawyers immediately for a free case consultation. Please use the form below to contact our …
Oct 18, 2021 · The product liability lawyers at Miller & Zois are actively seeking Similac NEC lawsuits from parents of premature infants who were fed with Similac (or another cow milk-based formula) and subsequently developed NEC. Call a Similac lawyer to talk about how we can help your family at 800-553-8082 or get a free online case evaluation. Contact Us
Apr 05, 2022 · Our law firm is currently seeking new preemie baby formula lawsuits to represent families who have suffered as a result of this infant formula. Our NEC formula lawyers are bringing lawsuits against the baby formula manufacturers. You can call our baby formula lawyers today in all 50 states at 800-553-8082. Time may be limited to bring an NEC lawsuit.
Parents are suing Enfamil manufacturer Mead Johnson and Similac manufacturer Abbott Laboratories because they knew or should have known their baby formula products could cause necrotizing enterocolitis (NEC) in premature infants. Manufacturers failed to warn parents and medical providers about the risk.
There was a Similac recall on February 18, 2022. This recall is for Similac, EleCare, and Alimentum manufactured in Sturgis, Michigan. This Similac recall comes on the heels of reports of Cronobacter sakazakii or Salmonella Newport in infants who had consumed these baby formula products made at the Michigan facility.
The exact cause of NEC is not fully understood, but there are many scientific and clinical studies definitively proving that cow-milk-based infant formulas, such as Similac and Enfamil, significantly increase the risk of a premature infant developing NEC. But the risk of NEC with premature babies has long been clear.5 days ago
Enfamil lawsuits are legal claims against Mead Johnson Nutrition for defective design and failing to warn consumers that its baby formula can cause preterm infants to get necrotizing enterocolitis (NEC). This serious gastrointestinal illness can result in lifelong complications and even death.Feb 18, 2022
"At this time, Similac PM 60/40 with lot code 27032K80 (can) / 27032K800 (case) are the only type and lots of this specialty formula being recalled," the FDA said. The recall comes after the CDC announced that another infant who had been exposed to the formula was infected with Cronobacter sakazakii.Mar 2, 2022
Similac, Alimentum, and EleCare powdered formula products recalled on February 17 have all three of these conditions: First two digits of the code are 22 through 37, AND. on the container contains “K8,” “SH,” or “Z2,” AND. Use-by date is 4-1-2022 (APR 2022) or later.Mar 25, 2022
Enfamil Increases the Risk of NEC in Premature Infants A growing body of scientific evidence has proven cow milk formulas like Enfamil significantly increases the risk of a life-threatening bowel infection called necrotizing enterocolitis (NEC) when given to premature infants.
around 3.5 million dollarsTo date, the average verdict or settlement of an NEC baby formula lawsuit is around 3.5 million dollars.Dec 9, 2021
The settlement amounts in these NEC lawsuits could be in the $250,000 to $750,000 range. In cases where the child endured a great deal of suffering but ultimately recovered, the the necrotizing enterocolitis compensation payouts may still be high.
Parents are now filing infant formula lawsuits across the country. These lawsuits allege that Mead Johnson failed to properly warn parents, physicians, and medical staff that Enfamil could significantly increase the risk of death or NEC in premature infants.
16, 2021, and Jan. 4, 2022. The recalled formula products were sold across the United States and in some other countries, according to the FDA. To identify them, look at the lot code, a multidigit number on the bottom of the container.Mar 2, 2022
The FDA is advising consumers to not use Similac, Alimentum, or EleCare powdered infant formulas if: The first two digits of the code on the container are 22 through 37. The code contains K8, SH or Z2. The expiration date is April 1, 2022, or later.Mar 2, 2022
Our infant formula attorneys are reviewing NEC lawsuits for families who have children that were: Using Similac or Enfamil formula Born prematurely...
A class action lawsuit or MDL has not yet been formed for the NEC baby formula lawsuits. But this inchoate litigation is just getting underway. As...
There has not been a recall for Enfamil or Similac. Our baby formula lawyers are not calling for a recall. Instead, our attorneys argue that this i...
The NEC infant formula lawsuits are just getting started. But we can estimate settlement amounts and compensation payouts from juries at trial by l...
Now keep in mind all those NEC settlements and verdicts were lawsuits were brought against doctors and hospitals. These are typically sympathetic d...
The cases with the highest value settlement amounts or trial value if this litigation is successful is the case where the child needs ongoing care...
The NEC infant formula litigation is just beginning. So also take predictions as to when you can expect settlement payouts with a grain of salt. B...
NEC is a very serious bacterial infection that can develop in the gastrointestinal system of newborn infants. It primarily occurs in premature or u...
These NEC baby formula product liability lawsuits are new. But families have been filing medical malpractice lawsuits in necrotizing enterocolitis...
No, the NEC baby formula lawsuits will not become a huge class action lawsuit. Thankfully, there number of victims is relatively small. NEC is rare.
The Schmidt Firm, PLLC is currently accepting baby formula induced injury cases in all 50 states. If your baby was born preterm or prematurely and developed Necrotizing Enterocolitis (NEC) after being fed baby formula in the NICU, you should contact our lawyers immediately for a free case consultation.
In February 2022, a recall was issued for Similac, Alimentum and EleCare powdered baby formula from a facility in Sturgis, Michigan, after the products were linked to a deadly infection outbreak.
For more than 30 years, the manufacturers of baby formula have known that it can significantly increase a premature baby’s risk of Necrotizing Enterocolitis (NEC), a life-threatening intestinal disease.
In recent years, a growing number of lawsuits have been filed by angry parents who accuse baby formula companies of downplaying the deadly risks of giving cow’s milk-based formula to an infant.
The label on Similac has no warnings about NEC, and only a vague warning that “very low birth-weight infants are particularly susceptible to gastrointestinal complications.” The label on Enfamil does not include a single warning about NEC or other intestinal complications.
No. Doctors and nurses in the Neonatal Intensive Care Unit (NICU) are not being sued. Instead, baby formula lawsuits are specifically targeted at manufacturers who are intentionally not warning about the dangers of feeding their products to preterm babies.
Similac lawsuits are being filed against Abbott Laboratories, Inc., the company that manufacturers and advertises all Similac infant formula, including products for premature infants.
Babies born prematurely require extra nutrition to boost their development and growth.
NEC is a very serious bacterial infection that can develop in the gastrointestinal system of newborn infants. It primarily occurs in premature or underweight infants.
Even a mild case of NEC can be very dangerous and potentially life-threatening for a premature baby. Between 15-40% of premature infants with NEC die. The main reason for this is that NEC can lead to a fatal blood infection called sepsis.
Even when NEC is not fatal, it can cause other long-term or permanent complications and adverse health consequences. 1 of every 3 babies with NEC will develop intestinal strictures.
NEC only occurs in 1 out of every 2,000 full-term live births in the U.S. In premature births, however, the condition is much more common. NEC occurs in about 10% of all premature babies (born 37 weeks or earlier).
A new study published on October 14, 2021, in the British Medical Journal will add new fuel to any necrotizing enterocolitis formula lawsuit. The study suggests that the makers of infant formulas such as Similac and Enfamil have funded biased and unreliable clinical product trials.
Similac is manufactured and sold by Abbott Laboratories Inc ., a large medical device and health care product company based in Illinois. You have likely heard of them. You are less likely to have heard of Mead Johnson Nutrition Company, the company that makes Enfamil. But it is a 16 billion-dollar company.
Unfortunately, studies have demonstrated that certain cow’s milk-based baby formulas might be doing these babies more harm than good. In particular, there are links to a crippling disease called Necrotizing Enterocolitis (NEC).
February 18, 2022 - FDA warns against powdered infant formula. Abbott recalls products. Three types of baby formula are being recalled after reports of bacterial infections.
We asked a group of 173 NEC (Necrotizing Enterocolitis) parents: How many weeks gestation was your baby born?
Two of the most prominent baby formula producers in the United States – Abbott Laboratories and Mead Johnson & Company – have had NEC lawsuits filed against them. The lawsuits claim that Abbot Laboratories’ product Similac and Mead Johnson’s Enfamil should have carried warning labels to make parents aware of the dangers to their newborns.
NEC is a gastrointestinal disease that causes inflammation and perforations (holes) in the intestines. This can lead to further problems when bacteria leaks through the hole and stomach and into the bloodstream. While NEC is always described as a “serious” illness, symptoms can range from mild to life-threatening.
NEC is mostly associated with preterm babies (around 9 out of 10 NEC cases are found in preterm babies), particularly those born before 28 weeks, but it can also occur after a child has received a blood transfusion or when the child is fed through the stomach (enteral nutrition).
Stage: IB Classification: Suspected NEC Systemic signs: Temperature instability, apnea, bradycardia, lethargy Intestinal signs: Bright red blood from rectum Radiologic signs: Normal or intestinal dilation, mild ileus
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To date, multiple lawsuits have been filed by parents after their children developed necrotizing enterocolitis by ingesting either Similac or Enfamil baby formula.
Necrotizing enterocolitis is a digestive disease that occurs primarily in premature infants and can cause inflammation of the intestinal lining, which can eventually lead to serious infections.
According to the scientific study, Similac and Enfamil products have been linked to digestive disease.
Abbott Laboratories, the maker of Similac, and Mead Johnson and Company, the company behind Enfamil, are currently being sued by parents whose children developed health issues after ingesting their baby formula products.
While not all baby formula products carry a risk of digestive disease, some cow milk-based products made by Enfamil and Similac do pose a risk to a child’s health. If you have any of the following products in your home, you should dispose of them and find a safer alternative for your child:
NEC primarily affects prematurely born infants, children born under 3.25 pounds, and newborns who are fed formula in their early life. The condition only occurs in every 2,000-3,000 births, but it’s especially dangerous to infants, as their immune systems have not developed enough to fight off harmful bacteria.
Neocate infant formula is made by Nutricia, a global company specializing in medical foods for people with allergies, metabolic conditions, and gastrointestinal disorders. Nutricia North America was established in 1983 and is headquartered in Rockville, Maryland. Nutricia North America is owned by parent company Groupe Danone based in Paris, France.
On a broader level, Neocate lawsuits inform other concerned parents and child advocates of dangers in the marketplace, while sending a message to regulators and manufacturers that we will not tolerate reckless disregard for safety in product development.
The amino acid-based formula is made from a basic, easily-digested, easily-absorbed protein to avoid triggering an allergic reaction. In addition to its line of infant formulas, Neocate also offers products for elementary school-aged children with food allergies up to age 12.
If no universal settlement agreement is reached through this process, the individual lawsuits may return to their court of origin for trial. No MDL has yet been formed for Neocate baby formula lawsuits, though consolidation is a possibility in the future. A Neocate MDL would differ from a Neocate class-action lawsuit.
Federal Food, Drug, and Cosmetic Act (FFDCA) [ 10 ] defines infant formula as "a food which purports to be or is represented for special dietary use solely as a food for infants by reason of its simulation of human milk or its suitability as a complete or partial substitute for human milk".
September 2010 – Abbott Laboratories recalled its Similac formula recall after the FDA said the product could cause internal discomfort and could lead infants to refuse to eat. Affected products included powdered formula (not liquid Similac), and were sold in either in plastic containers or in specific size cans including 8-ounce, 12.4-ounce, and 12.9-ounce cans.
November 2014 – Three lots of the probiotic ABC Dophilus were recalled in Nov. 2014 when a premature baby died after being given the supplement in a hospital , according to the U.S. Centers for Disease Control and Prevention (CDC). The agency determined that the affected product contained Rhizopus oryzae, a fungus that can cause a severe infection of the sinus, lungs, intestines and skin called mucormycosis.
Rhizopus oryzae is a common fungus found in decaying organic matter like leaves and rotting wood. An outbreak of mucormycosis of the skin caused by rhizopus oryzae occurred during the cleanup of the Joplin, Missouri tornado in 2011. According to a Solgar spokesperson, because the fungus is so ubiquitous, “the exact source of where this mold came from is extremely difficult to determine.” ABC Dophilus is made for Solgar by a contract manufacturer, but the company declined to name its supplier.