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.
Maserati is recalling 2017 Levante vehicles because an engine software issue may cause the transmission to shift into neutral or the engine to shut off at slow speeds.
Polaris is recalling 2017 Slingshot, SL, and SLR vehicles because three steering and suspension bolts may be insufficiently tightened, potentially reducing vehicle handling.
Jaguar Land Rover is recalling 2016 Range Rover and Range Rover Sport vehicles because the passenger air bag inflator may fail to ignite, preventing deployment in a crash.
Picone Meat Specialties is recalling approximately 5,750 pounds of pork salami products because they contain non-fat dry milk, a known allergen, that is not declared on the label.
King's Command Foods is recalling approximately 26,138 pounds of ground beef products due to possible contamination with extraneous materials, including metal objects.
Jaguar is recalling 2017 F-PACE vehicles with automatic transmissions because a short rear driveshaft may separate, causing loss of drive power and increasing crash risk.
Airstream is recalling 2017 Base Camp recreational trailers because heavy loads may cause tires to contact the wheel well liner, risking tire failure and crashes.
Gillig is recalling 2,732 Low Floor transit buses because wiper arms can crack and detach, reducing driver visibility and increasing crash risk.
Papa John's Salads & Produce is voluntarily recalling Colby Cheese Half Moons due to possible Listeria monocytogenes contamination.
ADM Milling Co. is recalling 25,000 pounds of ADM Polar Bear Flour because a product sample tested positive for salmonella. The flour was distributed in Illinois and Indiana.
JML Ingredients is recalling IQF Cut Green Beans in 20 lb cases due to potential Listeria monocytogenes contamination. The product was distributed in Massachusetts and Pennsylvania.
G&W Laboratories is recalling Indocin suppositories due to out-of-specification impurity results found during stability testing.
Windstone Medical Packaging is recalling 606 Shoulder Arthroscopy Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.
Papa John's Salads & Produce is voluntarily recalling Monterey Jack Cheese Half Moons due to possible Listeria monocytogenes contamination.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are recalled because splits or holes may compromise sterility.
Sunrise Growers is recalling organic IQF Dark Sweet Cherries due to possible Listeria monocytogenes contamination. The recall covers 1,800 cases distributed in California.
Olympus is recalling URF-P6 and URF-P6R uretero-reno fiberscopes due to adverse events involving tissue trauma and stuck insertion tubes reported in similar devices.
Hyundai is recalling 2011-2015 Sonata and Sonata Hybrid vehicles because front seat belt linkages may detach from anchor pretensioners, increasing injury risk in crashes.
United Exchange Corporation is recalling 190,710 bottles of Eye Wash due to a lack of assurance of sterility. The product was distributed nationwide, in Puerto Rico, and in Guyana.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions kits are being recalled because splits or holes may compromise sterility.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in AMS kits are recalled because splits or holes may compromise sterility.
AbbVie is recalling Duopa (carbidopa and levodopa) cassettes because stability testing showed the drug may settle near the end of its shelf life.
United Exchange Corporation is recalling 112,320 bottles of Eye Irrigating Solution because the product lacks assurance of sterility.
United Exchange Corporation is recalling 77,184 bottles of Eye Wash because the product lacks assurance of sterility. The recall covers specific lots distributed nationwide, in Puerto Rico, and in Guyana.
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in custom Aligned Medical Solutions arthroscopy kits are recalled because splits or holes may compromise sterility.