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.
Chicago Kimchee is recalling 1-gallon jars of Korea whole Kimchee due to undeclared anchovies, a major food allergen.
Impax Laboratories is recalling specific lots of Dextroamphetamine Sulfate Tablets because they failed impurity and degradation specifications.
Ford is recalling 2,288 model year 2016 F-250, F-350, F-450, and F-550 trucks because tires may have inner sidewall damage that could cause a blowout.
Ford is recalling 2014-2015 Explorers because rear suspension toe links may fracture, potentially causing loss of steering control and increasing crash risk.
Nissan is recalling 2013-2016 Sentra vehicles because a deformed seat belt bracket may prevent the front passenger air bag from turning off when a child seat is installed.
Toyne Inc. is recalling 2014-2015 Pumper emergency vehicles because a gearbox defect may cause the truck to shift into neutral while driving, increasing crash risk.
Nissan is recalling specific 2013-2017 Nissan, Infiniti, and Chevrolet vehicles because the passenger air bag may fail to deploy in a crash.
Pilgrim's Pride is recalling approximately 4.57 million pounds of fully cooked chicken products that may contain plastic, wood, rubber, or metal.
Pitts Enterprises is recalling 2014-2016 logging trailers because suspension welds may crack, causing the suspension to shift or detach and increasing crash risk.
Chrysler is recalling specific 2012-2015 Dodge, Chrysler, and Jeep vehicles because they may fail to warn drivers when exiting while in gear, posing a rollaway risk.
Winnebago is recalling 2014 Tour and Itasca Ellipse motorhomes because the brake signal to towed devices may not deactivate, causing dragging brakes and fire risk.
Vermeer is recalling 2015-2016 TLR33 trailers because undersized tires may rub against fenders, increasing the risk of sudden tire failure and a crash.
Kia is recalling 2016 Optima vehicles because the driver's frontal air bag may not deploy fully in a crash, increasing injury risk.
Hyundai is recalling specific 2015-2017 Sonata, Sonata Hybrid, and Elantra vehicles because the driver's frontal air bag may fail to fully deploy in a crash.
Terex is recalling 2001-2003 XT52, XT55, and XT60 aerial devices because lower booms may be made of insufficiently strong material, posing a risk of cracking and injury.
Customed, Inc. is recalling 18 units of Hip and Knee Replacement Surgical Packs due to inadequate sterilization validation and package integrity concerns.
Uoriki Fresh Inc is recalling Uoriki Octopus Salad packaged at Wegman's deli counters in New Jersey due to potential Listeria monocytogenes contamination.
Jayco is recalling 322 model year 2016 Octane Super Lite travel trailers because they may lack a 30-amp circuit breaker, increasing the risk of fire during an electrical short.
JRZ Dairy Products Inc. is recalling specific containers of Puredesi and Puredahi Low Fat Yogurt because the products were not pasteurized for the required length of time.
Dexcom Inc is recalling 18,004 G4 Platinum Pediatric Receivers because they may fail to provide intended audible alarms or alerts.
Northern Tier Bakery is recalling Tuna Salad Sandwiches sold in Minnesota and Wisconsin due to an undeclared milk allergen.
Dexcom Inc is recalling 41,925 G5 Mobile Receivers because they may fail to provide intended audible alarms or alerts to users.
Customed, Inc. is recalling 36 units of Laparoscopy-Gyn Surgical Packs due to inadequate validation of sterilization processes and package integrity.
Dexcom Inc is recalling G4 PLATINUM Receivers with Share because they may fail to provide intended audible alarms or alerts.
Customed, Inc. is recalling 15 units of Plastic Surgery Packs (Catalog Number 9001402) distributed in Puerto Rico due to inadequate validation of sterilization processes and package integrity.