Baby and kids' product recalls

The recalled 3 mm magnetic ball sets violate the mandatory standard for toys because the magnet sets contain loose magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

Potential for false resistant results for Colistin (cs02n) with multi-drug-resistant Pseudomonas aeruginosa and Acinetobacter baumannii complex used in specific cards

The recalled test kits contain a bottle of sulfuric acid, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The test kits violate the mandatory standard for child-resistant packaging because the bottle of sulfuric acid is not child-resistant, posing a risk of serious injury or death from poisoning, if the contents are swallowed by young children.

The recalled dressers are unstable, if they are not anchored to the wall, posing serious tip-over and entrapment hazards, that can result in injuries or death to children. The dressers violate the mandatory standard as required by the STURDY Act.

The recalled children's loungewear sets violate the mandatory flammability standard for children's sleepwear, posing a risk of burn injuries or death to children.

The toy airplane inside the egg contains levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues.

Potential physical contaminant

Potential peanut protein cross-contact.

Pieces of foam can present a choking hazard to a child, increasing the risk of injury.

The recalled blinds have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The blinds violate the federal rule for window coverings and present a substantial product hazard. In addition, the blinds also violate labeling requirements for window coverings.

The recalled shades have long operating cords and accessible inner cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The shades violate the federal rule for window coverings and present a substantial product hazard. In addition, the shades also violate labeling requirements for window coverings.

The numbing cream contains lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The numbing cream's packaging is not child-resistant, posing a risk of serious injury or death from poisoning, if the contents are swallowed by young children.

The cooling gel pads can become hot if left in the sun or a hot car, posing a burn hazard to young children.

Unapproved Drug Claims and Misbranded.

Unapproved Drug Claims and Misbranded.

Unapproved Drug Claims and Misbranded.

Unapproved Drug Claims.

The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in serious injuries or death to children. The dressers fail to meet the mandatory standard required by the STURDY Act.

The recalled baby loungers violate the mandatory standard for Infant Sleep Products. The sides are too low to contain an infant. The sleeping pad is too thick, posing a suffocation hazard. The enclosed openings at the foot of the loungers are wider than allowed, posing a fall hazard and an entrapment hazard to infants. Also, the baby loungers do not have a stand, posing a fall hazard if it is used on elevated surfaces. These violations create an unsafe sleeping environment for infants and can cause death or serious injury to infants. In addition, the recalled baby loungers come with crib bumpers, which are banned by the Federal Safe Sleep for Babies Act because the padded crib bumpers can obstruct breathing, posing a risk of serious injury or death to infants from suffocation.

The recalled kids' helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional stability, labeling and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.

The recalled toys violate the mandatory standard for toys containing button batteries because the compartment that holds the batteries in the remote can be accessed without the use of a common household tool. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns and death.

The potential for minor injury such as damage to the vessel and/or tearing of the vessel wall.

Potential for spoilage due to yeast contamination.

The recalled children's pajama sets violate mandatory standards for children's sleepwear flammability, posing a risk of burn injuries to children.

The recalled toy is intended for children under three years of age and contains small parts, which violates the small parts ban, posing a deadly choking hazard.

The recalled multivitamins contain iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The recalled packaging of the iron-containing multivitamins violates the federal standard for child-resistant packaging because the bottle caps are not child-resistant, posing a risk of deadly poisoning, if the contents are swallowed by young children.

The baby loungers violate the mandatory standard for Infant Sleep Products because the sides are shorter than the minimum side height limit to secure the infant; the sleeping pad's thickness exceeds the maximum limit, posing a suffocation hazard; and an infant could fall out of an enclosed opening at the foot of the lounger or become entrapped. The portable loungers do not have a stand, posing a fall hazard. These violations create an unsafe sleeping environment for infants, posing a risk of serious injury or death.

During an internal investigation, ACS determined that the rationale for sterilization of certain components was not justified and therefore, some components are not fit for further sterilization according to ACS procedures. As a result, ACS is unable to confirm product sterilization assurance requirements were met.

Foley catheter may have an obstructed lumen, which may result in an inability to drain the bladder, of urine and may include pelvic or abdominal pain, flank pain, bladder dysfunction, obstructive uropathy, acute kidney injury and/or hydronephrosis.

The recalled lite-up torches contain button cell batteries in violation of the mandatory standard for toys and the recalled mini laser pointers contain button cell batteries in violation of the mandatory standard for consumer products because the button cell batteries can be accessed easily by children. Additionally, the laser pointers do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.