TRUBLUE iQ and TRUBLUE iQ+ Auto Belays
Head Rush Technologies, of Louisville, Colorado
The recalled auto belay device can fail to retract, posing a fall hazard and risk of serious injury or death.
95,075 total recalls in our database
Head Rush Technologies, of Louisville, Colorado
The recalled auto belay device can fail to retract, posing a fall hazard and risk of serious injury or death.
Unknown Manufacturer
The wall sconce's electrical wires can become damaged at the adjustable joints, posing a risk of electric shock.
Unknown Manufacturer
The recalled childrenβs pajama sets and robes violate the flammability regulations for childrenβs sleepwear, posing a risk of burn injuries and death to children.
Burnsen SA, of Belgium
The boilers can release carbon monoxide (CO) due to delayed ignitions or component damage, posing a risk of serious injury or death.
Unknown Manufacturer
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.
Product contains undeclared sulfites (4.66 mg/serving).
United Natural Trading Inc.
Product mislabeled. The back label states Organic Cashews. The front product label states Wegmans Organic unsalted dry roasted almonds. The front label is correct label for this product.
Product contains undeclared FD&C Yellow 5 and FD&C Yellow 6.
Jack & The Green Sprouts
Sprouts have the potential to be contaminated with Listeria monocytogenes
Product contains elevated levels of lead - 6.50 mg/kg (ppm)
Undeclared allergen (soy).
FEEL GOOD FOODS
Foreign object (metal pieces).
Product contains undeclared sulfites (56.8mg/serving)
Glenmark Pharmaceuticals Inc., USA
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
Failed impurities/degradation specifications and Sub-potent Drug: Out-of-specification results were obtained during routine stability testing for Assay and Impurities.
Glenmark Pharmaceuticals Inc., USA
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
Glenmark Pharmaceuticals Inc., USA
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
Glenmark Pharmaceuticals Inc., USA
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
Glenmark Pharmaceuticals Inc., USA
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
Fagron Compounding Services
Lack of Assurance of Sterility