Baby and kids' product recalls

The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).

The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).

The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).

The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).

The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).

The forceps have been used in ways not covered by the design resulting in breakage of the clamps.

Chemical Contamination

Chemical Contamination

A missing recall registration card may result in an unregistered child seat, which can delay recall notification and increase the risk of injury.

The stools can collapse or tip over while in use, posing serious fall and injury hazards to children.

The recalled gates violate the federal safety regulations for expansion gates and expandable enclosures because a child's torso can fit through the opening between the gate and the floor, posing a risk of serious injury or death due to entrapment hazard.

Telcare, LLC has received customer complaints related to battery expansion/swelling for its Philips Connected Blood Glucose Meter (i.e., BGM 4 brand name) Monitoring System.. The issue was identified by post market surveillance data (customer complaints) - events of battery expansion/swelling and associated symptoms, e.g., leading to the device's removable back cover (battery port) to separate. If there is a loss of primary function of the device due to the described device defect, an immediate health consequence that may result is prolonged hypoglycemia or hyperglycemia due to delay in treatment, as the blood glucose measurement is not available to guide treatment. In a worst-case situation, there is potential for battery swelling to result in explosion of the battery and/ or device. Exposure to explosion, and subsequently projectiles from the explosion, may result in several immediate health consequences, including concussion, headache, dizziness, eye irritation, blurred vision, eye injury, and vision impairment.

Affected lot (439363) exhibited a negative dose drop of -22% with native patient samples compared to alternate reagent lots. Patient samples tested with the affected lot may demonstrate repeatable falsely decreased results, which may lead to improper diagnosis or repeat testing.

Due to foreign object: metal balls (tiny non-magnetic metal balls measuring less than 2mm inside the gummies) intended for children

An incorrect label may result in an improperly restrained child, increasing the risk of injury in a crash.

The recalled Taylor Water Technologies reagent bottles sold with test kits contain sulfuric acid, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging for the bottle with sulfuric acid is not child resistant, posing a risk of chemical burns to the skin or eyes and internal corrosive burns, if ingested.

The recalled crib bumpers violate the federal crib bumper ban, posing a deadly suffocation hazard to infants. Padded crib bumpers are banned by the federal Safe Sleep for Babies Act.

The recalled children's bathrobes violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries and death to children.

The recalled unassembled Deluxe Pit Kit slot cars violate the mandatory federal regulation for magnets because the magnets used to power the car are loose prior to assembly, posing an ingestion hazard to children. Assembled models do not pose this risk and are therefore not subject to this recall. When high-powered magnets are swallowed, the ingested magnets can attract each other, or another metal object, and become lodged in the digestive system. This can result in perforations, twisting and/or blockage of the intestines, infection, blood poisoning and death.

The recalled children's nightgowns, pajama sets and robes violate the federal flammability standards for children's sleepwear, posing a risk of serious burn injuries or death to children.

The stroller fan's housing allows consumers' fingers to contact the fan's blade, posing a laceration injury hazard to small children.

Firm received complaints of infant choking.

Firm received complaints of infant choking.

Undeclared Yellow #5

Undeclared Yellow #5

The recalled baby loungers violate the federal safety regulations for Infant Sleep Products because the sleeping pad is too thick, posing a suffocation hazard; an infant could fall out of an enclosed opening at the sides of the lounger or become entrapped; and the sides are too low to contain the infant and the loungers do not have a stand, posing a fall hazard. These violations create an unsafe sleeping environment for infants.

The recalled high chairs pose a fatal suffocation risk because they were marketed, intended, or designed for infant sleep, and they have an incline angle greater than 10 degrees in violation of the federal Safe Sleep for Babies Act. In addition, the high chair poses a deadly entrapment hazard because the opening between the seat and tray is large enough that a child can become entrapped in it, which is a violation of the federal regulations for high chairs.

The recalled children’s pajama sets and robes violate the flammability regulations for children’s sleepwear, posing a risk of burn injuries and death to children.

The recalled pajamas violate the flammability regulations for children's sleepwear, posing a risk of burn injuries to children.

Due to an error message that prevents users from utilizing carboxyhemoglobin saturation and methemoglobin saturation sensors on their monitor/defibrillator system.