Severity 3 of 5
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.
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.
Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Philips is recalling 2,016 Azurion interventional fluoroscopic x-ray systems worldwide due to software defects that may degrade image quality or lose geometry movements, potentially delaying therapy or causing procedural complications.
Cardinal Health is recalling specific Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Medline is recalling bleach wipes that may lose potency before expiration, potentially allowing pathogens to survive.
Medline Industries is recalling Micro-Kill Bleach Germicidal Wipes because reduced bleach concentration may compromise disinfection effectiveness.
Philips is recalling Azurion Rystem X-ray systems due to software defects that may degrade image quality or lose geometry movements, potentially delaying therapy or causing procedural complications.
Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Cardinal Health is recalling 602 Presource surgical kits because they contain MEDICOM Ritmed Neurological Sponges with unexpected endotoxin variability.
Shoolin Pharma Chem LLP is recalling Tadalafil USP 0.500 KG bags due to Current Good Manufacturing Practice (CGMP) deviations noted during an FDA inspection.
E-One is recalling specific 2025-2026 fire trucks because a hydraulic valve defect may prevent outriggers from extending or retracting, potentially delaying emergency response.
BioFire Diagnostics is recalling 2,370 pouches of the BIOFIRE Respiratory Panel 2.1 test due to an increase in false negative results.
OBP Medical is recalling ER-Spec Single-Use Vaginal Speculums because a burr on the plastic blade may create a sharp edge, posing a risk of injury to patients and providers.
Halcore Group is recalling 2025-2026 Horton ambulances because touchscreen failures may prevent emergency lights from activating, increasing crash risk.
TooyBing is recalling its Wooden Bead Stacking Toys because the wooden beads pose a choking hazard to children under three years old.
Hampton Bay Halwin 52-inch ceiling fans are being recalled because the fan blades can separate from the motor flywheel, posing impact and injury risks. About 9,460 units sold at Home Depot between January 2023 and October 2025 are affected.
Qabefy twin mattresses sold on Amazon are recalled because they violate the federal flammability standard, posing a fire hazard. Consumers should stop using them and contact Qabefy for a refund.
Fastbuy is recalling about 200 Zimtown portable gas and fuel cans because the spout closure is not child-resistant, posing burn and poisoning risks to children. No injuries have been reported.
Chrysler is recalling 2026-2027 Jeep, Ram, Chrysler, and Dodge vehicles because the rearview camera image may fail to display when reversing, increasing crash risk.
Shengsen Prank Sound Makers are recalled because the lithium coin batteries can be easily accessed by children, posing an ingestion hazard. About 667 units sold on Amazon from April 2024 through April 2026 are affected.
CuberShop Magnetic Stickerless Speed Cubes (model YJ MGC 5×5) are recalled because loose high-powered magnets in the packaging pose an ingestion hazard to children. No injuries have been reported.
DUMOS Nine-Drawer Dressers are recalled because they can tip over and entrap children if not anchored to the wall, violating the STURDY Act. Consumers should stop using unanchored units and contact DUMOS for a full refund.
Ritchey Design is recalling about 775 carbon bicycle forks because the alloy insert in the crown hole can come loose, letting an accessory fall onto the front wheel and cause a crash. No injuries have been reported.
COMMOWNER electric pressure washers (models HD14P-Z and HX18) are recalled due to shock and electrocution hazards from a missing built-in GFCI. No injuries reported; stop use and contact AZ Home Concept for a refund.
SUGIFT is recalling 13 electric pressure washers (Model LTBBHG006) because they lack a ground-fault circuit interrupter and have a short power cord, creating shock and electrocution risks. No injuries have been reported.