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.
Lisy Corp. is recalling Sazon Perfecta seasoning in 4 oz, 12 oz, and 24 oz packages because it contains undeclared soy.
Green Valley Drugs is recalling specific lots of sterile hormone injections due to a lack of assurance of sterility and quality control concerns.
D& S Herbals, LLC is recalling Super Power capsules because they contain sildenafil, an unapproved drug ingredient.
Green Valley Drugs is recalling Phosphatidylcholine and Sodium Deoxycholate Injection due to a lack of assurance of sterility in compounded products.
Heartware Inc. is recalling 3,544 HVAD Pump Implant Kits worldwide because the driveline connector may loosen.
Carson's Country Market is recalling Assorted Cookie Packs sold in New York due to undeclared walnuts, wheat, milk, and peanut butter.
FVS Holdings, Inc. dba. Green Valley Drugs is recalling 607 vials of Methylprednisolone Acetate and Marcaine Injection due to lack of assurance of sterility and quality control concerns.
Green Valley Drugs is recalling Taurine Injection products because the compounding pharmacy lacked assurance of sterility and had quality control concerns.
Heartland Gourmet is recalling gluten-free pizza crust mix labeled as dairy-free but containing milk. The recall affects 204 boxes distributed to schools, online, and retail in TX, MN, CO, and Canada.
Green Valley Drugs is recalling Phenylephrine Injection vials because the pharmacy could not ensure the products were sterile.
Wheeled Coach is recalling 2008 Dodge Sprinter 2500 ambulances because a faulty solenoid can cut power to critical safety and medical equipment.
Elite Trailer Manufacturing is recalling 2012 Livestock Gooseneck trailers because a manufacturing defect in the hydraulic brake actuator could cause a loss of braking ability.
Pierce is recalling 2007-2013 Velocity, Impel, and Dash CF emergency vehicles because door handle springs may be too weak to prevent doors from opening in a crash.
Brammo is recalling 2013 Empulse electric motorcycles because an incorrectly attached cable can cause electrical shorting, leading to power loss or fire.
General Motors is recalling 2013 Cadillac SRX vehicles equipped with 18-inch wheels because the wheel lug nuts may loosen, increasing the risk of a crash.
Ferrara Fire Apparatus is recalling 2011-2012 Igniter and Ultra firetrucks because brake chambers may leak, causing the parking brake to drag and overheat.
Isuzu is recalling 1,161 model year 2013 N-Series trucks because a transmission retaining ring may dislodge, potentially causing the vehicle to stall and increasing crash risk.
Cardinal Health is recalling 4,571 Presource Total Knee Kits because plastic packaging remnants may obstruct airflow in the filter.
Cardinal Health is recalling 4,571 Presource Major Abdominal Kits because plastic packaging remnants may lodge in the filter and obstruct airflow.
John Evans is recalling 380 model year 2013-2014 chassis and trailers because wheel lug nuts may not be properly torqued, posing a crash risk.
Hospira Inc. is recalling 259,050 vials of Furosemide Injection due to a loose crimp on the vial cap that compromises sterility assurance.
Hospira Inc. is recalling QUELICIN (succinylcholine chloride) Injection due to a loose crimp on the vial that compromises sterility assurance.
Cardinal Health is recalling 4,571 Presource PBDS Extremity Circulator Kits because plastic packaging remnants may obstruct airflow.
Cardinal Health is recalling 4,571 Presource PBDS kits because plastic packaging remnants may lodge in the filter and obstruct airflow.
Maple View Farm Ice Cream is recalling Carolina Crunch pints due to undeclared peanuts, almonds, and soy.