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.
Chrysler is recalling specific 2008-2010 Dodge and Chrysler vehicles because the ignition switch may move out of the run position, turning off the engine and disabling safety systems.
General Motors is recalling 2013-2014 Chevrolet Cruze vehicles because the driver's air bag inflator may rupture in a crash, potentially causing serious injury.
General Motors is recalling 2014 Chevrolet Corvettes because improper rear shock absorber welds may cause the tubes to separate, leading to sudden handling changes and increased crash risk.
Wolf Steel is recalling Napoleon GD3200-P and GD3200B-P propane gas fireplaces because the glass front can shatter, posing a laceration hazard.
Sherman Produce Co is recalling Schnucks walnuts in 10 oz. plastic trays due to potential Listeria monocytogenes contamination. The product was distributed in Missouri and Illinois.
John W Hollis Inc is recalling specific lots of Testosterone Cypionate for Injection because the products lack assurance of sterility.
John W Hollis Inc. is recalling Levocarnitine Solution for injection because the company cannot ensure the product is sterile. The recall covers specific lots distributed nationwide.
Scott and Trek are recalling 2011-2013 bicycles with specific SR Suntour front forks that can break, posing a crash hazard.
John W Hollis Inc is recalling Polidocanol 0.5% Solution for Injection because the products lack assurance of sterility.
John W Hollis Inc is recalling Methylcobalamin 1000 mcg injectable products because they lack assurance of sterility. The recall covers Lot # 1862 distributed nationwide.
John W Hollis Inc is recalling specific lots of Cyanocobalamin injection because the products lack assurance of sterility. The recall covers 2,650 mL distributed nationwide.
John W Hollis Inc is recalling 80 mL vials of Lipotropic Gold injectable products because they may lack sterility assurance.
Whole Foods Market Group Inc. is recalling 140 units of Thai Soba Noodle Salad because the product contains undeclared soy.
Mitsubishi is recalling 2007-2013 Outlander vehicles because a power steering tube may leak fluid, potentially causing loss of steering assistance.
John W Hollis Inc is recalling B-Complex/Adenosine Injectable Solution due to a lack of sterility assurance in the compounded aseptically filled products.
John W Hollis Inc is recalling MIC Plus B12 injectable vials because the products lack assurance of sterility. Consumers should stop using the affected lots immediately.
John W Hollis Inc is recalling compounded Papaverine HCl and Phentolamine Mesylate injectable products due to a lack of assurance of sterility.
Mitsubishi is recalling 2007 and 2009 Outlander vehicles because a transfer case oil seal may dislodge, causing transmission fluid loss and potential loss of vehicle control.
Anhing Corporation is recalling Caravelle Chili Powder because it may be contaminated with Salmonella. The recall covers 83 cartons distributed nationwide.
John W Hollis Inc is recalling compounded injectable products containing papaverine, phentolamine, and alprostadil due to a lack of assurance of sterility.
Daimler Trucks North America is recalling 2015 Freightliner trucks because axle manufacturing errors may create weak spots, increasing crash risk.
Convatec Inc. is recalling the Flexi-Seal Fecal Management System because it lacks FDA 510(k) clearance and its Auto-Valve feature is not performing consistently.
John W Hollis Inc is recalling specific lots of compounded injectable products containing papaverine, phentolamine, and alprostadil due to a lack of assurance of sterility.
Actavis Inc is recalling 6,913 packages of Vancomycin Hydrochloride Capsules because the drug is subpotent. The recall covers distribution across the United States.
John W Hollis Inc. is recalling specific lots of Mannitol 5% Solution for injection because the products lack assurance of sterility.