Searching CPSC consumer products, FDA food & drug enforcement reports, and USDA meat & poultry recalls — sorted newest first.
1,499 recalls found — page 38 of 63.
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to swimmers and bathers.
The recalled bicycle lights violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the bicycle lights 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.
The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.
The recalled bicycle lights violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the bicycle lights 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.
The elevator's StrikeLock hoistway door locking device can allow the elevator cab to move with a landing door open, posing a risk of serious injury or death due to fall and injury hazards.
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety standard as required by the STURDY Act.
If perishable food or beverages are stored in the container for an extended period of time, the stopper can forcefully eject when opened, which can result in serious impact injury and laceration hazards to the consumer.
Salmonella. The firm was notified by the North Carolina Department of Agriculture that the product test positive for Salmonella.
Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
Potential presence of Salmonella.
Potential presence of Salmonella.
Potential presence of Salmonella.
Potential presence of Salmonella.
Potential presence of Salmonella.
Potential presence of Salmonella.
Undeclared milk allergen.