Child Safety

Published on: January 20, 2024

FDA Questions Whether Applesauce Pouches Were Contaminated Intentionally

apple-sauce-544676_1280-e1703985234173 As we’ve previously related on this blog, the United States Food and Drug Administration has recalled three applesauce products. These products include WanaBana apple cinnamon fruit puree pouches, Schunks cinnamon applesauce pouches, and Weis cinnamon applesauce pouches. The recall stems from the FDA’s investigation of dozens of acute lead poisonings in children that are associated with these brands of cinnamon applesauce pouches and the FDA continues to investigate. If your child suffered lead poisoning and you suspect it due to his or her consumption of these apple sauces, you should call the seasoned Chicago-based lawyers of Moll Law Group. Billions have been recovered in cases around the nation with which we’ve been involved.

Call Moll Law Group About Contaminated Cinnamon Applesauce Pouches

Over 60 children under the age of 6 have tested positive for lead poisoning after consuming the applesauce in the United States. Some of these children have been found to have over 500 times the acceptable threshold for lead. Standard blood screenings, which are recommended by the CDC to reduce lead exposure under age 6, helped identify those children who had elevated lead levels.

The FDA Deputy Commissioner for Human Foods, Jim Jones, believes it’s possible that the contaminated cinnamon applesauce pouches were intentionally tainted with lead. He’s explained that the evidence points to an intentional act by someone who is part of the supply chain for the pouches, which were sold under three different brands made in a manufacturing facility in Ecuador. The FDA is inspecting that facility. He has suggested that perhaps the perpetrator didn’t understand the pouches would end up in a country with strong, enforced regulations.

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Published on: February 21, 2023

Several Brands of Children’s Pajamas Recalled Over Fire-Safety Concerns

By Moll Law Group

Recently, the Consumer Product Safety Commission posted notice of several recalls involving children’s pajamas. While the recalls involved various manufacturers, the products were widely available online through major retailers such as Amazon, Uncommon Goods, and Macy’s, as well as in boutique stores nationwide.

Why Are Children’s Pajamas Being Recalled?

According to various posts on the Consumer Product Safety Commission (“CPSC”) website, the manufacturers of the pajama sets issued the recalls because they failed to meet the federal flammability standards for children’s sleepwear. Under existing regulations, all children’s sleepwear for children over the age of nine months must be either flame-resistant or tight-fitting. Tight-fitting pajamas do not need to be flame-resistant because close-fitting clothes pose a much lower risk of catching fire. All children’s pajamas that were recently recalled were not tight-fitting and failed to comply with the CPSC’s flame-resistant requirements.

Which Children’s Pajamas Were Recalled?

While many brands of children’s pajamas have been subject to recalls over recent months, the most recent group of recalls affects the following brands:

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Published on: February 13, 2023

4.7 Million Fisher-Price Rock ‘n Play Sleepers Recalled

By Moll Law Group

Child in pajamas Fisher-Price recently recalled its Rock ‘n Play Sleepers. The sleepers are made for infants, and they allow for parents to place their babies in bassinet-like beds designed for easy and comfortable sleeping. These sleepers were recalled because infants have tragically died while rolling from their backs to their stomachs or sides while unrestrained. Consumers have been advised to immediately stop using the strollers and to get a refund from Fisher-Price if they own the sleeper. If your child was injured due to an experience with the Rock ‘n Play, you should give the liability lawyers of Moll Law Group a call as soon as possible. Thanks to our team, billions have been recovered in lawsuits after consumer injuries just like these.

Details of the Recalled Fish ‘n Play Product

Approximately 100 deaths have occurred in connection with this Fisher-Price product. Apparently, the deaths have almost always happened when infants have rolled around while in the sleepers, partially because the infants have been entirely unrestrained. Fisher-Price reported that in several of the reported instances, it has been unable to confirm the exact circumstances that caused the related death or injury.

Affected sleepers were sold at Walmart, Target, and online at Amazon. Fisher-Price put the product on the market in September 2009, and they have been sold for anywhere between $40 and $149 since then. As of January 9, 2023, it is illegal to sell or distribute the recalled product. All models of the Rock ‘n Play sleeper have been recalled. To receive a refund for the Fish ‘n Play, consumers can go to Fisher-Price website and submit a claim. The Consumer Product Safety Commission estimates that more than 4.7 million of the recalled Rock ‘n Play sleepers have been sold to U.S. consumers.

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Published on: January 15, 2023

Weighted Blanket Recalled Following the Deaths of Two Children

By Moll Law Group

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Target stores recently announced a recall of more than 200,000 Pillowfort weighted blankets following multiple reports that children can become trapped under the blanket. In a statement, Target explained that the blankets, which are specifically marketed towards children, “pose a risk of death by asphyxiation.”

The weighted blanket recall follows confirmed reports from parents that their children were able to open up the outer cover of the blanket and crawl inside, at which point they became trapped. According to a recent news report,two children died last year from suffocation after getting trapped inside the Pillowfort weighted blanket.

The Consumer Product Safety Commission and Target are both suggesting that customers who purchased a Pillowfort weighted blanket return the item to the store for a refund. Of course, for families whose children may have been injured or killed as a result of the recalled product, a refund of $40 isn’t a fair remedy.

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Published on: July 12, 2022

FDA Warns About Baby Neck Floats

By Moll Law Group

baby-g3f121741c_640 Sometimes baby neck floats are used on babies with spina bifida, spinal muscular atrophy (SMA) type 1, cerebral palsy, and Down syndrome. The United States Food and Drug Administration (FDA) recently issued warnings not to use neck floats with babies with special needs or developmental delays, even when interventions such as water therapy are being provided. If your baby was injured or killed by a baby neck float, you should call the seasoned Chicago-based lawyers of Moll Law Group.

Consult the Lawyers of Moll Law Group

Some neck floats, inflatable plastic rings worn around a baby’s neck, permit babies to float in the water freely. They can be marketed for premature infants or even as young as two weeks old. Parents and caregivers use the products during babies’ baths or when their baby is swimming as a physical therapy intervention because they have developmental disabilities or delays. Some manufacturers claim that using these neck floats allows for increased lung capacity, muscle tone, flexibility and motion range, and stimulation of the brain and nervous system. They claim they can build strength or promote development, but these claims are not fully supported.

The U.S. Food and Drug Administration (FDA) has warned parents and others not to use neck floats with babies, even for therapy, especially when babies have developmental delays or special needs, such as cerebral palsy, spina bifida, Downs syndrome or spinal muscular atrophy type 1. Using floats can lead to death or severe neck strain and injuries.

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Published on: March 3, 2022

Second Infant Died After Consuming Recalled Abbot Baby Formula

By Moll Law Group

baby-g909db3e6f_640-e1646267137939 Recently, Abbot Nutrition expanded its recall of baby formula after a second baby died from infection after consuming the formula Abbot Nutrition’s Similac PM 60/40 with a lot code 27032K800. Four reports of Cronobacter sakazakii infection have been reported in connection with products from the plant. If your baby was harmed, hospitalized, or died because of its consumption of Abbot Nutrition’s Similac, you should call the experienced Chicago-based product liability lawyers of the Moll Law Group about whether you have a claim against the manufacturer. Similac PM is specifically intended for infants that are helped by lowered mineral intake; the specific formula in question wasn’t included in a prior, February 17 recall for lots of Similac, Alimentum, and EleCare, powdered formulas, that were also produced at the same plant. No parent should have to go through the anguish of a baby who dies because of a formula that should have been safe.

Call the Seasoned Product Liability Lawyers of Moll Law Group About Your Lawsuit

The FDA has updated its website to investigate another illness due to another Cronobacter sakazakii, which is a rare and dangerous bacteria that causes serious medical complications, including blood infections. A child died after hospitalization and an infection with this germ may have contributed to his death. He had consumed Similac before becoming infected. While four infections involving Cronobacter sakazakii were reported to the FDA and the Centers for Disease Control and Prevention, a Salmonella Newport infection was also reported alongside the outbreak. The five infants who became sick were all hospitalized. Two died.

Following the second baby’s death, Abbott Nutrition recalled the powdered formula the baby had consumed. To determine whether you are using a lot of powdered formula that has been recalled, you can look at the 7-9 digit code and expiration at the bottom of the package. Take a look at whether the first two digits of the code are 22 -67, the code contains Z2, SH, or K8, and the expiration date is April 1^st or later. You can type in the code on the bottom of your package at Similacrecall.com to make sure it’s part of the recall.

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Published on: February 8, 2022

Recall of Youth All-Terrain Vehicles for Noncompliance with Safety Regulations

By Moll Law Group

child-ga845f3ba0_640-e1644290312265 On February 2, 2022, certain Maxtrade’s Youth Coolster Mountopz All-Terrain Vehicles (ATVs) were recalled. The recall was issued because the ATVs did not comply with the mandatory federal ATV standard for safety. Notably, youth ATVs didn’t abide by the maximum speed limit for these vehicles when they are meant for children. ATVs are sold for minimum ages 6, 10, 12, or teens. Additionally, some of these recalled ATVs have parking brakes that don’t work to stop the ATV from moving, which could result in an accident. If an ATV caused you or your child injury, you should consult the experienced Chicago-based product liability lawyers of Moll Law Group about whether you have a claim. Billions have been recovered in cases with which we’ve been involved.

Give Moll Law Group a Call to Discuss an ATV Injury Claim

The recall concerns Maxtrade’s Coolster Mountopz ATVs, models 3050-B, 3050-C, 3125-B2, 3125-CX-2, 3125-CX-3, 3125-XR8-U2, 3150-CXC, 3150-DX-4, 3175-S2, and 3175-U. They were sold in a range of colors and for a range of children’s ages between January 2007 through January 2021. They cost from $370 – $1,100.

The handlebars of these vehicles were stamped with “Coolster.” As a parent, you can look at the model numbers in the center of the rear axle to figure out whether your child’s vehicle was affected. Around 141,000 ATVs were recalled. Consumers have been told to immediately stop using the recalled ATVs. You can contact Maxtrade for a repair from an authorized repair stop.

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Published on: September 30, 2021

Chicago-Based Lawyers for Magnet Ingestion Claims

By Moll Law Group

magnets-113315_1280-300x225 Children in Chicago and elsewhere are often extremely curious. They may put things in their mouths that are dangerous or should not be consumed. Among the many attractive products that may intrigue kids are magnets, whether refrigerator magnets or magnetic spheres or toys that contain magnets. They may be drawn by a bright color or by a toy’s magnetic properties. In August 2021, Zen Magnets and Neoballs Magnets were recalled because they posed an ingestion hazard. If you suspect your child has swallowed a magnet or more than one magnet, it is crucial to take him or her to receive emergency care. You may be concerned about the bills. Many families do not have enough money to cover the hospital bills or care required by the injuries suffered due to magnets. You should discuss what happened with the experienced Chicago attorneys of the Moll Law Group. Billions have been recovered in cases with which we’ve been involved.

Recall of Zen Magnets and Neoballs Magnets

When a child swallows two or more high-powered magnets, whether accidentally or intentionally, the magnets that were consumed may be attracted to each other or a different metal object. They could become lodged in the child’s digestive system. The presence of the magnets can result in twisting or blockage of the intestines, along with blood poisoning and death.

The mandatory recall involved both Zen Magnets and Neoballs magnets, which are highly powerful spherical magnets that are 5 mm in diameter. Neoballs are sold in a range of colors, including green, red, purple, blue, silver, gold, and orange. They were packaged with “Neoballs’ or “Zen Magnets” printed on the package. In total, around 10 million magnets, packaged individually and in sets, were recalled.

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Published on: September 27, 2021

Boppy Company Recalls More than 3 Million Infant Loungers

By Moll Law Group

baby-784609_640-300x199 The United States Consumer Product Safety Commission (CPSC) recently announced an alarming recall of which Chicago parents and parents around the country should be aware. The Boppy company recalled more than 3 million loungers for infants and newborns based on suffocation risks. The recalled lines include Pottery Barn Kids Boppy Newborn Loungers, Boppy Preferred Newborn Loungers, and Original Newborn Loungers. If your baby was suffocated and suffered injuries or death while using a Boppy lounger, you should call the experienced Chicago child injury attorneys of the Moll Law Firm about whether you have a case against the manufacturer or others in the chain of distribution.

Risk of Suffocation

Babies can be suffocated when placed in a Boppy or another infant lounger in a position that allows them to move or roll. They can also suffocate if they roll off a lounger onto another surface such as soft bedding or pillows on an adult bed. According to the CPSC, between December 2015 and June 2020, 8 infants suffocated after they were set on their stomachs, sides, or backs in Boppy loungers. They were discovered lying on their stomachs or sides.

Three million loungers for infants and newborns were recalled on September 23. In the United States, 3.3 million loungers have been sold in the United States. In Canada, Boppy sold 35,000 of these loungers. The loungers cost between $30-$44. They were sold January 2004 – September 2021.

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Published on: September 20, 2021

Recall of Children’s Cutie Spoovel Utensils

By Moll Law Group

cooking-4299302_1280-300x199 Parents in Chicago and around the country should be aware that recently, Ryan and Rose recalled the Cutie Spoovel utensil. The Cutie Spoovel is a transitional tool little kids use to eat, and it can present a danger. The handle of the Cutie Spoovel utensil can break off; this results in the release of small parts, posing a choking hazard for young children. The tool comes in two colors and is fashioned from a plastic core sheathed in silicone. The back of the spoon identifies the utensil as made by “Cutie Spoovel” and RR is printed on the handle back.

The manufacturer received three separate reports that the Cutie Spoovel utensil’s handle broke when a child bit down on it. Neither injuries nor choking have been reported. The Consumer Product Safety Commission (CPSC) advised all recalled utensils should be removed from children. They should be disposed. The company can be contacted for either a full refund or a $20 shop credit.

In addition, if your child suffered injuries because of a Cutie Spoovel or other utensil for children, you may be able to recover damages in a product liability lawsuit. These lawsuits are brought when a person who used the product is injured by a defect in it. You and your child might be able to recover compensation if your child was injured by a defective Cutie Spoovel utensil or another child tool.

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