Severity 4 of 5
Illness, injury, or structural failure has been reported. 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.
Abbott Laboratories is recalling Batch 26811Z200 of Abbott EleCare Infant Formula Unflavoured due to consumer complaints involving Cronobacter sakazakii and Salmonella Newport in infants.
The Medtronic TurboHawk Plus Directional Atherectomy System (catalog THP-S) is being recalled due to design similarities to another device that experienced tip detachment and embolization. The recall affects 245 devices distributed nationwide.
Concord Farms is recalling Fresh Enoki Mushrooms due to Listeria monocytogenes contamination found by the California Department of Public Health. The affected product was distributed in California and Nevada.
American Health Packaging is recalling one lot of Oxycodone Hydrochloride Oral Solution due to impurity failure detected at initial testing of the repackaged product.
Abbott is recalling Similac infant formula due to possible contamination with Cronobacter sakazakii and Salmonella Newport. The recall covers approximately 103,025 cases distributed nationwide and worldwide.
Custom Wheel House LLC is recalling specific Method Race Wheels because the spokes may crack under heavy loads, potentially causing a loss of vehicle control.
ev3 Inc. is recalling the Medtronic TurboHawk Plus Directional Atherectomy System due to design similarities to a device with reported tip detachment and embolization incidents. The FDA has classified this as a Class I recall.
Abbott Similac Human Milk Fortifier pouches are recalled due to potential Cronobacter sakazakii and Salmonella Newport contamination. The recall affects infants who may have received contaminated product.
Abbott is recalling Similac 360 Total Care Infant Formula due to consumer complaints of Cronobacter sakazakii and Salmonella Newport in infants, with Cronobacter found in the manufacturing facility.
Abbott Laboratories is recalling Similac 360 Total Care Sensitive Infant Formula due to potential Cronobacter sakazakii or Salmonella Newport contamination. The recall affects products distributed in the United States and worldwide.
Abbott is recalling multiple Similac infant formula products due to potential contamination with Cronobacter sakazakii and Salmonella Newport. These pathogens pose serious health risks to infants.
Winnebago is recalling certain 2022 Micro Minnie, Minnie, and Voyage travel trailers because the coupler was improperly welded, which may cause the trailer to separate from the tow vehicle and increase crash risk.
Kia is recalling 2014-2016 Cadenza vehicles because the front windshield may not be properly bonded, posing a risk of detachment.
Great Dane is recalling 2022 Champion and Everest trailers because suspension bolts were not properly tightened, posing a crash risk.
Chrysler is recalling 2021–2022 Dodge Durango and 2022 Jeep Grand Cherokee vehicles due to steering gear defect. The rack bar may have been insufficiently hardened, potentially causing loss of steering control.
Chrysler is recalling specific Mopar steering rack assemblies because the rack bar may bind, causing difficulty steering or loss of control.
Ford is recalling 2016-2018 F-150, 2016-2017 Expedition, and Navigator vehicles because a brake master cylinder leak may reduce front brake function and increase crash risk.
Forest River is recalling certain 2022 travel trailers due to improperly welded couplers that may cause trailer separation from the tow vehicle. Dealers will replace the coupler at no charge.
Vicinity Motor Corporation is recalling 2020-2021 Vi38 vehicles because the power steering gear box may become damaged, resulting in a loss of steering control.
Norco Industries is recalling certain frames with Model CA-5400 couplers due to improper welding that may cause trailer separation.
Daimler Trucks North America is recalling 2020-2023 Thomas Built Buses Saf-T-Liner EFX school buses because passenger seat mounting bolts may break, increasing injury risk in a crash.
Celltrion DiaTrust COVID-19 Ag Rapid Test kits from lot COVGCCM0008 are being recalled due to reports of false positive results. The affected 243 kits were distributed to six states before the recall.
GOLDEN MEDAL MUSHROOM INC is recalling Xuerong brand enoki mushrooms contaminated with Listeria monocytogenes. The affected product was distributed in California, Texas, and Illinois.
Maintainer is recalling 2021-2022 crane-equipped truck bodies because an inductor may contact the frame, causing an electric arc and increasing fire risk.
A limited number of Philips Respironics V60 ventilators were assembled with expired adhesive. If the adhesive fails, the ventilator could stop providing ventilation.