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.
Dierbergs Markets is recalling Classic Pinwheel Appetizer Wrap Platters due to undeclared anchovy, a potential allergen hazard for sensitive consumers.
SCA Pharmaceuticals is recalling Epinephrine HCl 4 mg in 0.9% Sodium Chloride 250 mL due to a lack of assurance of sterility and potential for leaking.
SCA Pharmaceuticals is recalling 130 bags of fentanyl citrate injection due to a lack of assurance of sterility caused by potential leaks in the sodium chloride bags used.
SCA Pharmaceuticals is recalling specific lots of Hydromorphone injection syringes because they may leak and lack assurance of sterility.
SCA Pharmaceuticals is recalling Bupivacaine HCl 0.1% bags due to a lack of assurance of sterility and potential for leaking.
MixBin Electronics is recalling liquid glitter iPhone cases because the contents can leak and cause skin irritation or chemical burns.
Timken is recalling specific rear hub unit bearings for 2011-2017 Ford Explorer 4X2 vehicles because they lack a self-retention feature, which could cause the wheel to separate.
Carli Suspension is recalling adjustable track bars for specific Ram trucks because a joint may break, causing loss of steering and increasing crash risk.
Vantage Mobility International is recalling 2017 Chrysler Pacifica lowered floor vehicles because rear pinion brackets may crack, causing wheel wobble and potential loss of control.
Daimler Vans USA is recalling 2010-2011 Freightliner and Mercedes-Benz Sprinter 2500 and 3500 vehicles because passenger air bag inflators may rupture during deployment.
Dana is recalling Spicer D-Series and E-Series steer axles because the castellated nut may not be properly torqued, allowing the tie rod to loosen and potentially disconnect.
Daimler Vans USA is recalling 2012 Freightliner and Mercedes-Benz Sprinter 2500 and 3500 vehicles because the passenger air bag inflators may rupture during deployment, posing a risk of serious injury or death.
Nestlé Waters is recalling about 12,300 AccuPure floor-standing filtration dispensers because they can overheat, smoke, or catch fire. No injuries have been reported.
Daimler Vans USA is recalling 2007-2009 Dodge and Freightliner Sprinter 2500 and 3500 vehicles because passenger air bag inflators may rupture in a crash.
YouBar is recalling Cashew Cherry Whole Food Bars because the cashew butter ingredient is under recall for potential Listeria monocytogenes contamination.
YouBar is recalling Dr. Morrison Coconut Cacao Bars because the cashew butter ingredient is under recall for potential Listeria monocytogenes contamination.
YouBar is recalling GDBA Protector Bar - Vanilla Coconut protein bars because the cashew butter ingredient is under recall for potential Listeria monocytogenes contamination.
YouBar is recalling Oatmeal Raisin Nutrition Bars because the cashew butter ingredient may be contaminated with Listeria monocytogenes.
PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection due to a media fill failure that compromised sterility assurance.
YouBar is recalling Nutrifuel Figgilicious Nutrition Bars because the cashew butter used in them may contain Listeria monocytogenes.
PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection due to a media fill failure that compromised sterility assurance.
YouBar is recalling POZZIBLE protein bars because the cashew butter ingredient is under recall for potential Listeria monocytogenes.
YouBar is recalling Paleo Protein Vanilla Coconut bars because cashew butter used in them may contain Listeria monocytogenes.
Mazda is recalling specific 2003-2008 models because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.
GnuPharma Corp. is recalling GnuPharma Relief 100% Herbal Supplement because one ingredient failed identity testing and two failed microbiological testing for E. coli.