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.
Rabbit Creek Products Inc. is recalling Paddy's Pub Classic Beer Bread Mix because it may contain flour contaminated with E. coli O121.
Treehouse Foods is recalling multiple brands of peanut butter dark chocolate protein bars due to potential contamination with Listeria monocytogenes from sunflower seeds.
Rabbit Creek Products is recalling Flower Pot Parmesan Southwest Beer Bread Mix because it may contain flour contaminated with E. coli O121.
Treehouse Foods is recalling Nature's Harvest Sunflower Kernels, Ranch Flavored, due to potential contamination with Listeria monocytogenes.
Treehouse Foods is recalling Nice! Peanut Lovers Trail Mix because it may contain sunflower seeds contaminated with Listeria monocytogenes.
Treehouse Foods is recalling specific Amport Foods and Naturally Select nut trail mixes because they may contain sunflower seeds contaminated with Listeria monocytogenes.
Greenberg Fruit Co is recalling diced potatoes labeled 'Joe's Pride' because routine environmental tests detected Listeria monocytogenes on processing machines.
Hyundai is recalling 2015-2016 Sonata and Sonata Hybrid vehicles because the panoramic sunroof panel may detach while driving, creating a road hazard.
REV Ambulance Group is recalling 39 ambulances from 2016-2017 because defective seat tracks may allow attendant seats to move rapidly during a crash, increasing injury risk.
Newmar is recalling 2015 Dutch Star motorhomes because the brake signal to towed devices may not deactivate, causing dragging brakes, overheating, fire, or crashes.
Hyundai is recalling 2010-2016 Genesis Coupe vehicles because the front passenger air bag sensor connector may dislodge, potentially causing incorrect air bag deployment in a crash.
Autocar is recalling 1,132 model year 2015-2017 Xspotter and Xpert vehicles because improperly tightened steering linkage nuts could cause loss of steering.
Autocar is recalling 2,375 Xpeditor trucks because steering linkage nuts may be loose, risking loss of steering and crashes.
Summer Infant is recalling Lil' Luxuries infant bath tubs because the fabric slings can detach, posing risks of impact injury and drowning.
Mack Trucks is recalling 57 model year 2017 Pinnacle CHU and CXU trucks because improperly cured tires may cause partial tread separation, increasing crash risk.
Jayco is recalling 137 model year 2017 Seismic travel trailers because an incorrect fuse may fail to protect the circuit, increasing the risk of an electrical fire.
Continental is recalling specific Crosscontact LX20 tires due to insufficient adhesion that can cause tread loss and increase crash risk.
Pharmacy Plus, Inc. is recalling Pre-Op Pledget Soln + Tetracaine vials because the agency cannot ensure the product is sterile.
Bounce Life Style HQ is recalling Apple Cinnamon Protein Energy Balls due to potential Listeria monocytogenes contamination from sunflower kernels.
Pharmacy Plus, Inc. is recalling 139 vials of Hydroxyzine HCl injection in Mississippi due to a lack of assurance of sterility.
Pharmacy Plus, Inc. dba Vital Care Compounder is recalling Buprenorphine 0.6 mg/ml Injection due to lack of assurance of sterility.
Pharmacy Plus, Inc. dba Vital Care Compounder is recalling 62 vials of Trypan Blue 0.3% due to a lack of assurance of sterility.
The FDA is recalling Autologous Serum Tears from Vital Care Compounder due to a lack of assurance of sterility. The product was distributed in Mississippi.
Pharmacy Plus, Inc. dba Vital Care Compounder is recalling C-PAP/PHEN/PROST/ATROP 150/5/5 injection vials due to a lack of assurance of sterility.
Pharmacy Plus, Inc. dba Vital Care Compounder is recalling C-PAP/PHEN/PROST/Atrop 150/7.5 injection vials due to a lack of assurance of sterility.