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.
Johnson Health Tech is recalling about 19,900 Matrix T1 and T3 Series commercial treadmills because the power cord can become loose from the power socket, causing sparking, smoking, melting, and fire. No injuries have been reported.
Tesla is recalling certain 2016-2022 Model S and X, 2017-2022 Model 3, and 2020-2022 Model Y vehicles. The Full Self-Driving (Beta) software rolling stop feature may allow vehicles to pass through all-way stop intersections without stopping, increasing crash risk.
Chrysler is recalling 2019-2020 RAM 2500-5500 vehicles because wiper arms may loosen, reducing visibility in certain weather conditions.
GM recalls certain 2021 Tahoe, Suburban, Yukon, and Escalade vehicles for rear driveshaft assemblies with improperly heat-treated internal components that may fail, causing loss of drive power and increased crash risk.
Certain 2019-2021 Audi vehicles are recalled for rear axle misalignment that may cause premature tire wear and increase crash risk. Dealers will inspect and adjust the alignment at no charge, replacing any worn tires as needed.
Covidien is recalling 66 SonarMed AirWave Monitor Kits because the alarm may fail to sound and sensors may be incorrectly detected as disconnected, potentially causing the monitor to stop monitoring patients without alerting staff.
Draeger Medical recalls 26 Fabius MRI Anesthesia Machines due to incorrectly routed internal oxygen hoses. The misrouting can cause oxygen flow to deviate from set levels, risking inadequate patient oxygenation.
Toyota is recalling certain 2021 Venza Hybrid vehicles due to water intrusion in rear turn signal lights, which can cause electrical short circuits and lighting failure, increasing crash risk.
Straumann USA LLC is recalling certain Neodent Easypack dental implant kits due to mislabeling where packaging does not match the implant dimensions inside. Affected units contain 3.5x8mm implants instead of the labeled 3.5x13mm size.
Eguana Technologies is recalling about 245 Evolve Home Energy Storage Systems because the lithium-ion battery modules can overheat and pose a fire hazard. Consumers should contact the company immediately to schedule a free repair or battery replacement.
Geri-Care Pharmaceuticals is recalling about 800 bottles of over-the-counter acetaminophen and aspirin tablets because the packaging is not child resistant, posing a poisoning risk to young children.
Gentueri Inc is recalling 4,150 units of Gentueri Viral Transport Medium (VTM) nationwide due to visual turbidity and discoloration that may compromise diagnostic samples in transit.
Ortho-Clinical Diagnostics is recalling VITROS High Sample Diluent A Reagent Pack Lot 2190 because it produces lower than expected TSH test results. The recall affects 1,416 units distributed worldwide.
Konica Minolta's ImagePilot versions 1.92 and 1.93 software may provide incorrect measurement calculations if improper power sequences are used with AeroDR or Momentum Panel systems.
Aroma Meats LLC is recalling Nethili Pickle products distributed in Oregon because the label fails to disclose that the product contains anchovy, a common food allergen.
Compass Health Brands is recalling 3,734 Voyager Rollator walkers due to cracking wheel spokes that may cause wheels to separate from the axle, potentially resulting in patient falls and injuries.
Microbiologics Inc is recalling KWIK-STIK and LYFO DISK microbiological reference products contaminated with Staphylococcus epidermidis. Fifty-nine kits were distributed to multiple U.S. states and countries.
Straumann USA LLC recalls Neodent Easypack Helix GM Acqua dental implants due to mislabeling. Implants have incorrect dimensions compared to carton labels, which could affect surgical planning and placement.
AOSKERA is recalling approximately 1,000 children's nightgowns sold on Amazon.com from October 2020 through May 2021 because they fail to meet federal flammability standards for children's sleepwear, posing a burn injury risk.
Stanley Security Solutions is recalling 11 Senior Living Arial Emergency and Nurse Call Systems because they fail to alarm due to increased memory consumption, potentially preventing nursing staff from responding to resident emergencies.
Sensis cardiac diagnostic systems used in catheterization and electrophysiology procedures are recalled due to a software error (version VD12A) that can temporarily disable cardiac output measurement. No illnesses have been reported.
Philips North America recalls Cardinal Infant Heel Warmers because labeling was changed without FDA approval. The devices cannot be sold or distributed without new FDA clearance.
Greiner Bio-One is recalling 889,200 blood collection tubes (Lot #B21053QG) due to variation in lithium heparin that may cause blood clotting. The tubes were distributed to ten U.S. states.
Forest River is recalling specific 2021-2023 transit buses because a failed relay module can increase the risk of a fire. Dealers will install a wire jumper harness free of charge.
Certain 2021 Harley-Davidson motorcycles may not display the speedometer or neutral indicator at startup in freezing temperatures, creating a crash risk. Owners should contact Harley-Davidson for a free software update.