Severity 4 of 5
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
RL Schreiber Inc is recalling Demi-Glace Brown Sauce Mix because it was manufactured with flour potentially contaminated with E. coli.
Ohio Hickory Harvest Brand Products Inc. is recalling 25 lb. bags of Rucker's Cajun Mix due to potential Listeria monocytogenes contamination.
Cantrell Drug Company is recalling 935 vials of Hydromorphone HCl 50 mg/50 mL single-dose syringes due to a lack of assurance of sterility.
LSG Sky Chefs is recalling FRESH TO GO Mediterranean Chicken with Hummus sandwiches due to potential Listeria monocytogenes contamination from a recalled hummus ingredient.
Cantrell Drug Company is recalling 80 bags of Calcium Chloride 1 g/50 mL due to a lack of assurance of sterility.
Request Foods Inc. is recalling GFS Cheese Manicotti in tomato sauce due to undeclared eggs. The product was distributed in Michigan, Ohio, Florida, and Kentucky.
Cantrell Drug Company is recalling 30,796 syringes of Phenylephrine HCl 1 mg/10 mL due to a lack of assurance of sterility. The recall covers products distributed nationwide.
Cantrell Drug Company is recalling specific lots of Neostigmine Methylsulfate injection syringes because the firm cannot ensure the products are sterile.
Cantrell Drug Company is recalling 2,681 bags of Oxytocin 30 USP Units due to a lack of assurance of sterility. The affected product is distributed nationwide.
Mary's Homemade Vegetable Soup is being recalled because it is underprocessed and may pose a Clostridium Botulinum hazard.
Cantrell Drug Company is recalling 162 syringes of Lidocaine HCl 1% because the firm cannot assure the sterility of the product.
Green Cuisine, Inc. is recalling Pesto Pasta Salad with Arugula because it may be contaminated with Listeria monocytogenes.
Troyer Cheese Inc is recalling Backroad Country Peanut Butter Pretzels due to potential Listeria monocytogenes contamination. The product was distributed to 26 states.
First Source LLC is recalling specific lots of Oriental Snack Mix due to potential Listeria monocytogenes contamination. The product was distributed to retail stores in 11 states.
Cantrell Drug Company is recalling 93 vials of Hydromorphone HCl injection solution nationwide due to a lack of assurance of sterility.
Apple Tree Goat Dairy is recalling all lots of its 8 oz and 5 lb Chevre products due to potential Listeria monocytogenes contamination.
First Source LLC is recalling multiple varieties of Fitness Mix due to the potential for Listeria monocytogenes contamination. The product was distributed to retail stores in 11 states.
Publix Super Markets is recalling Danish Maple Walnut Coffee Cake strips due to the presence of small metal shavings.
Cantrell Drug Company is recalling 73 bags of Calcium Chloride in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Cantrell Drug Company is recalling specific lots of Succinylcholine Chloride 200 mg/10 mL injection syringes because the firm cannot ensure the products are sterile.
Topnotch Foods is recalling Regular Bread Crumbs in bulk bags because they contain undeclared egg, tree nuts, and milk.
Cantrell Drug Company is recalling 87 bags of Ropivacaine HCl 0.25% due to a lack of assurance of sterility. The product is intended for epidural use only.
Volkswagen is recalling 2009-2010 Jetta, GTI, Golf, and Audi A3 vehicles because the ABS control unit may fail, potentially causing loss of vehicle control.
Zebra Technologies is recalling approximately 166,000 power supply units for thermal printers due to a fire hazard caused by overheating and corrosion.
Aria Child is recalling about 29,400 gb Qbit strollers because a hinge gap can pinch hands and the stroller may fold unexpectedly, posing injury risks.