Searching CPSC consumer products, FDA food & drug enforcement reports, and USDA meat & poultry recalls — sorted newest first.
1,498 recalls found — page 7 of 63.
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and drowning hazards to swimmers and bathers.
The recalled nursing pillows advertised for infant feeding and tummy time violate the mandatory safety standards for nursing pillows?and infant support cushions?because they can obstruct an infant's breathing, posing a serious risk of injury or death from suffocation.
The recalled drain covers violate the entrapment protection standards of the?Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and drowning hazards to swimmers and bathers.
The affected interlock switches can become stuck in a retracted position, allowing the exterior door to remain unlocked, posing a risk of death or serious injury if the elevator is called to another floor.
The recalled tents' fiberglass poles can shed fibers, posing an injury risk of skin and eye irritation.
The hard plastic outer shell can bubble or partially peel off, resulting in loose pieces of film-like plastic that pose a choking hazard to young children.
The recalled heater's fan blade can detach from the motor shaft, which can cause the fan to slow or stop, leading to overheating and melting of the enclosure and internal parts. Melted internal parts can ignite and breach the enclosure if the thermal cut off or fuse does not timely activate, posing a fire hazard.
The recalled Wyze Solar Cam Pan security cameras' incorrect assembly instructions can lead consumers to accidentally puncture the lithium?ion battery's metal casing, causing the battery to rapidly overheat, posing a risk of serious injury or property damage from fire and burn hazards.
Product may contain metal fragments.
Presence of Foreign Substance
Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.
Presence of Foreign Substance.
Presence of Foreign Substance.
CGMP Deviations
sub potency
CGMP Deviations
CGMP Deviations
Chemical Contamination: contamination with a diluted propylene glycol-based coolant from a machine leakage during the packaging process.
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Potential physical contamination: dark spot was noticed on the bottom of container.
Cross Contamination with Other Products: due to a potential for cross-contamination with Acemetacin API due to an issue at the API manufacturer.
Improperly eviscerated which may result in Clostridium botulinum contamination
Incorrect product formulation: bag did not contain copper and famotidine per label.