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.
International Motors is recalling 2022-2027 IC Bus EVSB school buses because a high voltage disconnect switch may fail to shut off power, posing a risk of electrical shock.
BISSELL Steam Shot OmniReach and Omni handheld steam cleaners are recalled after 206 reports of hot water or steam escaping from the attachments, including 161 reports of burn injuries.
Osprey 700 Max and S1 robotic pool vacuums are recalled because the lithium-ion battery can overheat. Ten reports of overheating or fire have caused nine incidents of property damage; no injuries reported.
Nissan is recalling 2009-2010 Cube vehicles because the driver's air bag inflator may rupture or detach during deployment, posing an injury risk.
Honda is recalling certain 2018-2022 Odyssey vehicles because a software programming error can cause the side and side curtain air bags to deploy unexpectedly. 440,830 vehicles are affected.
Philips Respironics is recalling the Trilogy Evo O2 ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Philips Respironics is recalling the Trilogy Evo Universal ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Philips Respironics is recalling the Trilogy Evo ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
One lot of Magnesium Sulfate in Water for Injection is being recalled after a foil pouch labeled as magnesium sulfate was found to contain an IV bag of tranexamic acid.
Imu-Tek Animal Health has recalled Imu-Tek Colostrum-5 Powder because the product may be under-processed. The recalled lot was distributed across 29 states.
Lone Star Dairy Products LLC is recalling Spray Dried Dairy Powder in 25 kg bags and 1 metric ton totes due to Salmonella identification in finished product testing.
Baxter is issuing an urgent correction for the Blue Ventilator Adapter Module used with the Volara system because home users may be unaware of possible oxygen desaturation or lung injury from overexpansion.
Abiomed is recalling Automated Impella Controllers because the Purge System Blocked alarm display could be delayed when using first generation Impella 5.5 pumps.
Philips Respironics is recalling the Trilogy EV300 ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Purge Cassettes sold within Impella Pump Sets and individually packaged are being recalled because of an increased risk of purge leaks with Generation 1 purge cassettes.
Bombardier Recreational Products is recalling 2025 Can-Am Origin electric motorcycles because a front brake caliper support may fail, causing inoperative front brakes.
Mercedes-Benz is recalling specific 2018-2020 E-Class and S-Class models because the drive shaft universal joint may break, causing a sudden loss of drive power and increasing crash risk.
Graco is recalling specific SnugRide Turn & Slide infant seats because the carrier may detach from the base in a crash, increasing injury risk.
E Mishan & Sons is recalling Granitestone Diamond Pro Blue sauté pans because the metal cap on the handle screw can detach and forcefully eject when heated. One injury has been reported.
Huizhou Haitan Technology is recalling T400 battery chargers because they can ignite or cause a connected battery to ignite. Thirty-three fires and explosions have been reported.
Sleepy Customs LLC is recalling IS300 Slave Cylinder Conversion Kits because the adapter plate may separate, causing loss of clutch function and increasing crash risk.
Samson International is recalling Universal Broadmoor Bellevue and Oaklynn canopy bed frames because the canopy beams can collapse. Four consumers sustained contusion injuries.
Sevillo Fine Foods is recalling Slow Roasted Diced Tomatoes (24 lb bulk packages, UPC 00823338008216) because the product may contain metal fragments.
Philips Respironics is recalling the Trilogy Evo ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Distribuidora de Alimentos Sendero LLC is recalling Gorditas de Azucar (UPC 860010238134) distributed in Texas because the product labels do not disclose wheat and soy allergens.