Articles Posted in Product Liability

Recently, Bayer recalled 6 mL size Afrin Original Nasal Spray bottles because of the danger they pose to cause severe injury or illness from child poisoning. The bottles violate the mandatory standard for child-resistant packaging. The sprays contain an imidazoline; under the Poison Prevention Packaging Act, this substance must be placed in child-resistant packaging or meet label requirements for noncompliant packaging. If your child was injuries by one of the recalled Afrin nasal sprays, you may be able to recover damages. To determine whether you have a viable claim, you should call the experienced product liability attorneys of the Chicago-based Moll Law Group. Billions have been recovered in cases around the country with which we’ve been involved.

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Only the 6 mL bottles of Afrin nasal spray are affected by the recall. The recall applies to around 786,100 bottles. They were sold between September 2024 to April 2026 for $7 – $9 at convenience stores and travel hubs, such as airports. The problem with the noncompliant packaging of the 6 mL nasal spray is that it isn’t child resistant and it also doesn’t carry a required labeling statement. These problems present a risk of serious injury or illness if a child swallows the contents of the bottles.

Affected by the recall are unexpired 6 mL (travel-size) bottles of Travel Size Afrin Original Nasal Spray from Lot numbers 230361, 240822, 241198, 250066, 250152, 250646, and 250831. The containers have “Afrin® Original Nasal Spray” and “1/5 FL OZ (6 mL)” printed on a label that is on the front of the bottle. This is a six-digit number, after which is the expiration date in the format of “YYYYMMM.”

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On April 30, 2026, 5.8 million Thermos Stainless King 3000 and 3020 Food Jars and 2.3 million Thermos Sportsman 3010 Food & Beverage Bottles were recalled by the manufacturer. They are dangerous because when perishable beverages and food are stored inside them for a long period and then opened, the stopper may forcefully eject, which can result in serious injuries, including the danger of lacerations, to a consumer. If you were injured by one of the affected Thermos jars or bottles, you should call the seasoned Chicago-based product liability attorneys to see whether you have a viable claim. Billions have been recovered in cases with which we’ve been involved around the nation.

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Thermos has gotten 27 reports of consumers who were hit by a forcefully ejected stopper when the jar or bottle was opened. In some cases, the laceration or impact injuries necessitated medical attention. Three people experienced permanent vision loss after being hit in the eye by the stopper.

The bottles and jars were sold at Walmart, Target, and other retail stores around the country around March 2008 and July 2024. Additionally, they were sold in the same time frames on Amazon.com, Thermos.com, Target.com, and Walmart.com.

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Sizing catheters, made in many different lengths and configurations, are used to address a range of patients’ angiographic procedures, aortic interventions, peripheral interventions and vascular interventions. These catheters have marker bands that are used to appropriately orient the catheter within a patient’s body. The tips come in “straight,” “PIG,” and “VCF,” and the catheters can be up to 100 cm. Recently, the manufacturer Cook Medical sent a letter to impacted customers that recommended specific sizing catheters be removed from their sales point or site of usage. The affected catheters are the Centimeter Sizing Catheters, the Aurous Centimeter Sizing Catheters, and the Beacon Tip Centimeter Sizing Catheters. Cook Medical has advised that the affected sizing catheters should not be used. The FDA has since issued a recall. If you or a loved one was injured by a sizing catheter, call the seasoned Chicago-based lawyers of Moll Law Group. Billions have been recovered in cases with which we’ve been involved around the nation.

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On April 2, Cook Medical sent out a letter to tell affected customers that they should examine their inventory to figure out whether they had affected products and quarantine those affected products that weren’t already used. The company had found that the marker bands on specific catheters could be at an increased risk of breaking or cracking.

Customers were also told not to distribute or use whatever was remaining of the affected products. Adverse events related to the sizing catheters can be reported to Cook Medical Customer Relations by phone at 800.457.4500 or 812.339.2235, Monday through Friday between 7:30am and 5:00pm (Eastern Time), or by email to: CustomerRelationsNA@CookMedical.com.

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Several different models of Nexgrill grill brushes were recalled recently. It was found that the small metal wire bristles in those brushes could detach from the grill brush and attach to the grill or to food. This presents a danger of ingestion, and consequently, the danger that someone could suffer serious injuries, including ones that necessitate surgery. If you were injured as a result of Nexgrill grill brushes sticking to your food, you should call the seasoned Chicago-based product liability lawyers of Moll Law Group. Billions have been recovered in cases with which we’ve been involved around the country.

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Nexgrill has become aware of a minimum of 68 reports and reviews that state that the grill brushes’ small wire bristles detached. There were five reports of people who swallowed the metal bristles and needed medical care to get the bristles removed from their throat or digestive tract.

The recalled grill brushes, which are between 18 and 21 inches long, and have the word “Nexgrill” on them, were sold at Home Depot and online at homedepot.com from 2015 through 2026 for $5 to $15. They have black plastic or wood handles.

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Recently, 4our Kiddies tip restraint kits, which include plastic tip restraints, were recalled because it was discovered that they could degrade or break. They present tip over and entrapment dangers that could cause serious injuries or even death to children or older people who were engaged with furniture secured to the wall with the restraints. If you or your child was injured as a result of a tip-over or entrapment caused by 4our Kiddies tip restraint kits, you should call the seasoned Chicago-based lawyers of Moll Law Group. Billions have been recovered in cases with which we’ve been involved around the country.

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The 4our Kiddies tip restraint kits, which has plastic tip restraints or furniture straps, were sold on Amazon.com from June 2019 through January 2026 for $6 to $21. They were recalled on March 26, 2026, because they may have a hidden defect.

The Consumer Product Safety Commission has become aware of a minimum of 150 cases where consumers reported that the plastic tip restraint kits broke. Three of these cases involved tip-over accidents.

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The FDA has reported that, based on medical device maker Abbott Laboratory’s company data, there have been 860 serious injuries connected to the recall of certain glucose monitoring sensors. Internal testing at the manufacturer determined that certain sensors can offer incorrect readings of low glucose. The consequences of this may involve injuries, complications, or even death. If you were harmed by one of the FreeStyle Libre 3 and FreeStyle Libre 3 Plus sensors, you should call the seasoned Chicago-based product liability lawyers of Moll Law Group. Billions have been recovered in cases around the nation with which we’ve been involved.

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In November 2025, Abbott issued a medical device correction, reporting that there had been 736 severe adverse events and deaths connected to certain affected glucose monitors. These events and deaths occurred on an international scale. When incorrect glucose readings go without detection, inappropriate treatment decisions for diabetic people may be made. For example, patients may consume excess carbohydrates or may skip or delay insulin doses.

Around 3 million Libre 3 and Libre 3 Plus sensors from a specific production line, around half of which were used or have expired were affected. The FDA issued an early alert in December. In January, the FDA classified it as a Class I recall, which is the most serious type of recall, on January 14, a company spokesperson told Reuters. Class I recalls occur when an affected product could cause serious injury or death if consumers continue to use it.

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