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.
Heartland is recalling 2016-2017 Torque travel trailers because the safety chains are rated for less weight than the trailer's gross vehicle weight rating.
Nissan is recalling 2016 Maxima and Murano vehicles because a damaged O-ring in the ABS actuator may reduce brake fluid pressure, increasing crash risk.
Toyota is recalling 2016 RAV4, Lexus RX350, and ES350 vehicles because a damaged O-ring in the ABS actuator may cause improper brake fluid pressure control, increasing crash risk.
Pilgrim's Pride is recalling fully cooked chicken nuggets that may contain plastic. No illnesses have been reported.
Deca International is recalling GolfBuddy BB5 GPS bands because charging ports can produce an electrical charge that burns exposed skin. Two consumer burn reports have been received.
Cruiser RV is recalling 2016-2017 Stryker travel trailers because the safety chains are rated for less weight than the trailer's gross vehicle weight rating.
Kanan Enterprises is recalling Favorites Natural Pistachios because the supplier notified them the product may contain Salmonella. The recall affects 408 cases distributed to five states.
ViewRay is recalling 5 MRIdian Radiation Therapy Systems due to a software defect that may fail to prompt users to shift the couch to a new isocenter during re-optimization.
Walter's Pharmacy is recalling specific lots of Cefazolin 50 mg/mL Ophthalmic Solution because the sterility of the product cannot be assured.
Lipari Foods, Inc. is recalling raw whole shelled pistachios due to potential Salmonella contamination. The products were distributed to retail and foodservice establishments in 14 states.
Walter's Pharmacy is recalling specific lots of Edetate Disodium 2% Ophth Solution because the sterility of the product cannot be assured.
Paradise Farm Organics Inc is recalling specific Thai Fusion products due to undeclared milk, a major allergen.
Fresh Creative Foods is recalling H-E-B Tartar Sauce because it contains undeclared fish due to a labeling error.
Healthy Solutions LLC is recalling Super Elixir Pouches due to potential Salmonella contamination. The affected product was distributed in California.
Walter's Pharmacy is recalling Silver Nitrate 1% Ophthalmic Solution due to a lack of assurance of sterility. The product is distributed in Pennsylvania.
Walter's Pharmacy is recalling two bottles of Acetylcysteine 10% Ophthalmic Solution due to a lack of assurance of sterility. The product was distributed in Pennsylvania.
Walter's Pharmacy is recalling Lidocaine Nebulizer 1% Solution because the product lacks assurance of sterility. The recall affects five bottles distributed in Pennsylvania.
ProSupps USA LLC is recalling Mr. Hyde Intense Energy Pre-Workout supplements because they may contain the undeclared non-dietary ingredient Picamilon.
Ukrop's Homestyle Foods is recalling approximately 2,881 pounds of ready-to-eat turkey, pork, and beef products due to possible contamination with foreign matter.
ProSupps is recalling Dr. Jekyll Intense Pump Pre Workout due to potential mislabeling and the presence of the non-dietary ingredient Picamilon.
Walter's Pharmacy is recalling Tobramycin 15mg/mL Ophthalmic Solution because the product lacks assurance of sterility. The recall affects specific lots distributed in Pennsylvania.
Walter's Pharmacy is recalling Lidocaine Nebulizer 2% Solution because the product lacks assurance of sterility. The recall affects 5 bottles distributed in Pennsylvania.
Dr. Reddy's Laboratories is recalling 3,342 vials of Zoledronic Acid Injection due to defective seals that may compromise sterility.
Siemens is recalling 124 SOMATOM Emotion and Sensation CT systems due to a potential malfunction in cardio licenses that could hazard patients and personnel.
Jack and the Green Sprouts, Inc. is recalling 5 oz packages of alfalfa sprouts that may be contaminated with E. coli 0157. The products were distributed in Minnesota, Wisconsin, and North Dakota.