All Recalls

The teeth of the recalled ascenders can fail to engage, making it difficult or impossible for the user to ascend.

The recalled sling carriers violate the safety requirements of the Safety Standard for Sling Carriers, including requirements for structural integrity and occupant retention, posing a fall hazard to babies. Additionally, the sling carriers pose a suffocation hazard because they fail to meet the federal safety standard's requirements for restraint systems, as the waist restraint can be used without the crotch restraint. Further, there are no warnings or instructional literature providing information to caregivers about keeping the baby's face clear to prevent suffocation or safe positioning, to prevent the baby from curling into a position with their chin resting on or near their chest. Sling carriers manufactured after January 30, 2018 are subject to the mandatory federal safety standard.

The recalled conditioner can contain bacteria, including Pseudomonas aeruginosa, an environmental organism found widely in soil and water. People with weakened immune systems or external medical devices who are exposed to Pseudomonas aeruginosa face a risk of serious infection that may require medical treatment. The bacteria can enter the body if inhaled, through the eyes, or through a break in the skin. People with healthy immune systems are usually not affected by the bacteria.