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.
Pirelli is recalling specific P7 Cinturato tires because incorrect maximum inflation pressure markings may cause tire failure and increase crash risk.
Cummins is recalling L9 diesel engines because remote fuel filter hoses may separate, causing fuel leaks, engine stalls, and increased fire or crash risks.
Polaris is recalling about 4,200 Ranger XD and Crew XD recreational off-road vehicles because door handles can stick, causing doors to unexpectedly open while the vehicle is moving. This poses a risk of occupant ejection and crashes.
Veyer is recalling about 64,000 WorkPro Momentum office chairs because bolts can fail, causing a fall hazard. Seven incidents have been reported with two minor injuries.
Ivy City is recalling approximately 700 children's pajamas that violate federal flammability standards. The pajamas pose a risk of burn injuries to children.
Samurai Mini Smoke Alarms sold by HSN can malfunction and fail to alert consumers to a fire. About 328,000 units from July 2020 through November 2024 are affected.
Vornado Air recalls about 7,780 VH2 Whole Room Heaters sold on Amazon because the power cord can partially detach, risking electric shock and fire. No injuries have been reported.
About 122 HallyBee Farmhouse 5-Drawer Dressers sold on Amazon from September 2023 to October 2024 are recalled due to tip-over and entrapment hazards when not anchored to a wall, risking injury or death to children.
Lexmark is recalling about 43,510 MS725dvn and MX725adve specialty printers because a metal part can dislodge and cause fire. One fire has been reported, though no injuries or damage resulted.
Jaguar is recalling 2019-2020 XE vehicles because wiring damage may prevent the rearview camera from displaying an image, increasing crash risk.
Land Rover is recalling certain 2023 Discovery Sport, 2023-2024 Defender and 2023 Range Rover Evoque vehicles because the centre console touchscreen may go blank at startup, failing FMVSS 111.
General Motors is recalling certain 2025 Chevrolet Equinox EV all-wheel drive vehicles because incorrect brake module software may stop adaptive cruise control engaging the brakes as expected.
Marion Body Works is recalling 2024 Spartan Fire Metro Star vehicles because a missing mechanical stop may allow the cab tilt cylinder to overextend, increasing the risk of injury.
GE Medical Systems is recalling approximately 928 Tec 820 SEV anesthesia vaporizers due to a manufacturing defect that can cause them to deliver less anesthetic agent than the dial setting indicates. The devices are distributed nationwide and globally.
GE Medical Systems is recalling 644 Tec 820 ISO Anesthesia Vaporizers due to a manufacturing issue that causes them to deliver less anesthetic than the dial setting indicates. Distributed nationwide and globally.
Granules Pharmaceuticals is recalling Metformin ER 500 mg tablets due to discovery of a Paracetamol tablet in one bottle. Patients taking the affected lot should verify their medication with their pharmacy.
GE Healthcare Optima XR240amx systems with column replacement may have missing bolts in the Column Safety mechanism. If these bolts are missing and the counterpoise cable fails, the X-ray arm could drop.
Certain GE Tec anesthesia vaporizers (Tec 6 Plus and Tec 800 series) may deliver less anesthetic agent than the dial indicates due to a manufacturing issue. Users should cease use and contact GE Medical for instructions.
Stryker's Neptune 3 and Neptune S Rover surgical suction systems are recalled due to improperly tightened bolts on the vacuum pump filter housing. Loose bolts may cause loss of suction force during medical procedures.
Jubilant Draximage is recalling 5,209 kits of Technetium Tc 99m Sulfur Colloid Injection that failed stability specifications. The affected lots (C2300070, C2300070E) were distributed nationwide.
Spacelabs Healthcare's Xhibit Telemetry Receiver (Model 96280) may experience a Windows proxy issue causing the system to restart and go offline for 1-1.5 minutes, creating a temporary gap in patient monitoring.
HP Hood is recalling Wellsley Farm Vanilla Non-Fat Greek Yogurt due to possible plastic foreign objects in some packages. Consumers should not consume the affected product.
Nipro Renal Solutions USA is recalling Citric Complete dry citric acid concentrate due to mislabeled outer cases that show incorrect potassium and calcium content values.
Aerin Medical is recalling 479 units of VivAer Stylus (Lot #10235) due to incorrect programming in units from a single lot. When connected to the Aerin Console, affected devices will be incorrectly identified as RhinAer Stylus.
Amerisource Health Services LLC is recalling Clobazam 10 mg tablets due to the presence of foreign tablets or capsules in some packages. The recall affects 5,178 cartons with Lot #1019594 distributed nationwide.