95,018 total recalls in our database
Tulkoff Food Products
Tulkoff Food Products Inc., 2229 Van Deman Street, Baltimore MD 21224 has initiated a recall of Tulkoff Spicy Kimchi Aioli, 18 fl oz Clear Plastic Squeeze bottle, item number 098001, lot number 09.18.2021M because of undeclared allergens (Soy, Wheat)
Undeclared egg and milk
Interstate Food Products
Product samples tested positive for Listeria monocytogenes. The products also contain undeclared soy lecithin.
Lakeview Farms
Potential Listeria monocytogenes contamination in fish
The Leavitt
Product may contain high levels of aflatoxin.
EL PRESIDENTE FOODS
FDA inspection at foreign manufacturer found that peanuts exported to US in November 2020 contained non-approved Red #6
Subpotent
NSNY Distributor
Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/ or tadalafil
DIBAR NUTRICIONAL S DE RL DE CV
Chemical Contamination: FDA analysis found 3 lots of DiBAR hand Sanitizer to be below the label claim for ethanol content and to contain methanol.
DIBAR NUTRICIONAL S DE RL DE CV
CGMP Deviations: Other lots and products of hand sanitizer recalled because they were manufactured under the same conditions as the product lots found to contain methanol.
DIBAR NUTRICIONAL S DE RL DE CV
CGMP Deviations: Other lots and products of hand sanitizer recalled because they were manufactured under the same conditions as the product lots found to contain methanol.
CGMP Deviations: Other lots and products of hand sanitizer recalled because they were manufactured under the same conditions as the product lots found to contain methanol.
NSNY Distributor
Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/ or tadalafil
Philips North America
Significant wear of the Monitor Bracket Assembly shaft goes unrecognized could potentially lead to the Monitor Bracket Assembly detaching from the Suspension Arm and result in potential hazard for the monitor to fall while remaining attached to the cables resulting in patient, operator, bystander, or service person to serious injury.
Philips North America
Significant wear of the Monitor Bracket Assembly shaft goes unrecognized could potentially lead to the Monitor Bracket Assembly detaching from the Suspension Arm and result in potential hazard for the monitor to fall while remaining attached to the cables resulting in patient, operator, bystander, or service person to serious injury.
Magellan Diagnostics
Magellan has received reports that control tests of either the Low-Control and/or the High-Control generated a low result. The issue may cause the underestimation of blood lead levels in patient samples.
There is a potential that the pressure tubing may detach from the blood sampling system
Philips North America
Significant wear of the Monitor Bracket Assembly shaft goes unrecognized could potentially lead to the Monitor Bracket Assembly detaching from the Suspension Arm and result in potential hazard for the monitor to fall while remaining attached to the cables resulting in patient, operator, bystander, or service person to serious injury.
Synaptive Medical
Due to visible burrs/metal filings affixed along the suction tube inner perimeter.
Philips North America
Significant wear of the Monitor Bracket Assembly shaft goes unrecognized could potentially lead to the Monitor Bracket Assembly detaching from the Suspension Arm and result in potential hazard for the monitor to fall while remaining attached to the cables resulting in patient, operator, bystander, or service person to serious injury.