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.
Polestar is recalling certain 2025 Polestar 3 vehicles because the panoramic glass sunroof may not be properly secured and can detach, becoming a road hazard and increasing crash risk.
Aterian is recalling approximately 194,400 PurSteam Elite Travel and Mighty Lil Steamers because they can expel hot water, causing serious burns. The company has documented 54 burn injury reports, including two second-degree burns.
Clark Associates has recalled about 158,486 aluminum outdoor chairs and barstools whose legs can bend or break during use. The company received 36 reports of broken or bent legs, resulting in four falls and three injuries.
Superfoods, Inc. is recalling Live it Up Super Greens dietary supplement powder nationwide due to potential Salmonella Typhimurium contamination affecting 795,834 units.
Superfoods, Inc. is recalling Live it Up brand Super Greens dietary supplement powder nationwide due to potential Salmonella Typhimurium contamination. The recall affects approximately 795,834 units.
The Broselow Pediatric Emergency Tape contains dosing errors for emergency medications including Vecuronium, Flumazenil, and Ketamine, potentially affecting pediatric emergency care calculations.
SunMed Holdings is recalling the Broselow Domestic Complete ALS Organizer due to potentially harmful dosing errors for three critical medications used in pediatric emergency care. Vecuronium, Flumazenil, and Ketamine dosages may be incorrect on the reference tool.
SunMed Holdings is recalling the Broselow Organizer due to potentially harmful dosing errors for pediatric emergency medications Vecuronium, Flumazenil, and Ketamine. Approximately 89 units have been distributed worldwide.
SunMed Holdings is recalling Broselow Pediatric Emergency Rainbow Tape due to potentially harmful dosing errors for critical emergency medications used in pediatric care.
Ford is recalling 2025 Super Duty pickups (F-250, F-350, F-450) due to improperly welded steering column shifters that may detach. A detached shifter prevents shifting into park, risking unintended vehicle rollaway.
Ford is recalling certain 2020-2021 Explorer and Aviator vehicles because seat belt buckle anchor bolts may be improperly secured, potentially failing to properly restrain occupants during a crash.
The rear axle drivetrain welds in certain 2024 Mercedes-Benz eSprinter vehicles may fail, causing loss of drive power and increasing the risk of a crash or vehicle rollaway.
Volvo is recalling 2025 EX30 vehicles because the high-voltage battery may short circuit and overheat, creating a fire risk. Owners should park outside away from structures and limit charging to 70% until repairs.
The AiTuiTui Pull String Teething Toys pose a choking hazard from detachable string tentacles. About 49,410 units were sold on Amazon from August 2022 to September 2025; 15 choking incidents have been reported.
White Castle Original Sliders may contain undeclared milk and soy allergens. Approximately 1,021 cases distributed to Illinois, Ohio, and Texas with best-by date April 18, 2026.
Anthony's Barbecue & Dip-It Sauce contains an undeclared fish allergen (anchovy from Worcestershire). The product poses a serious risk to consumers with fish allergies.
Medline Industries is recalling Full Electric Lightweight Homecare Beds due to a fire hazard in the hand control pendant. The pendant may overheat under certain operating conditions and pose a risk of fire.
Medline is recalling Full Electric Basic Homecare Beds because the hand control pendant may overheat and catch fire in rare scenarios. The company has received 58 complaints of pendant sparking, burning, melting, or fire.
Medline is recalling Full Electric Low Basic Homecare Beds due to a fire hazard in the hand control pendant. The pendant may overheat under certain operating conditions, creating a risk of fire.
Medline is recalling 13,245 Semi Electric Lightweight Homecare Beds because hand control pendants may overheat and pose a fire risk in certain conditions. The company has received 58 reports of pendant sparking, burning, melting, smoking, or fire.
Medline Industries recalls homecare beds due to fire risk in the hand control pendant. The pendant may overheat and ignite, posing a fire hazard to users.
Medline is recalling 373,392 Semi Electric Basic Homecare Beds due to hand control pendants that may overheat and pose a fire risk. The company has received 58 complaints of pendant sparking, burning, melting, and smoking.
Yetonamr Pull String Teething Toys sold on Amazon are being recalled because silicone strings can lodge in the throat, creating a choking hazard. The CPSC is aware of 32 choking incidents.
HerbsForever Gastro Care herbal supplement may contain undeclared wheat, posing a risk to consumers with wheat allergies. The recall affects product batch 124-4 distributed online nationwide.
One Roof LLC is recalling Atwater's Holiday Cookie Tin (19.65 oz) due to undeclared tree nut allergens including almonds, pecans, and walnuts. The recall affects 197 containers distributed to Maryland.