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.
Tesla is recalling certain 2021 Model X and Model S vehicles because the driver's air bag cushion may tear during deployment, potentially failing to protect occupants in a crash. Tesla will replace the air bag free of charge.
Keystone RV Company is recalling 2022 Arcadia fifth wheel travel trailers because the Federal Identification Label contains incorrect tire size and pressure information. This could lead to over-inflation and increase the risk of crashes.
Autocar is recalling 2019-2022 Xpeditor vehicles because the hazard lights will not function with the ignition turned off. This violates federal safety standards and could increase crash risk in hazard situations.
Kia Motors America is recalling 2020-2021 Stinger vehicles with a fuel gauge software error that may cause inaccurate readings, risking unexpected fuel depletion and vehicle stalling.
Yamaha is recalling 2016-2021 FJR1300 motorcycles because a previous software update may prevent the engine from accelerating as intended, increasing crash risk.
Tiffin Motorhomes is recalling certain 2018–2022 recreational vehicles with sofa seat belts that may not be correctly installed. Unsecured passengers face increased injury risk in a crash.
Cottrell is recalling 2019-2022 2-Car Carriers because four side-rear reflex reflectors are missing, which reduces visibility and increases crash risk.
Mercedes-Benz is recalling certain 2021 GLB250 and AMG GLB35 vehicles because the driver-side window airbag may not be properly mounted to the A-pillar, which could prevent proper deployment during a crash.
Kubota is recalling about 48,875 RTV-X1100C utility vehicles from model years 2013 through 2021 because floor mats can warp or degrade and interfere with the throttle pedal, creating crash and injury risks.
Tracker Marine is recalling 2022 Ranger Trail boat trailers because improperly spaced fenders may contact tires, causing premature wear and potential tire failure.
Supreme is recalling 2019-2020 Dry Freight Body vehicles because a rearward-aiming license plate light may increase crash risk.
Backyard Play Systems is recalling four outdoor playset models due to an entrapment hazard in the wooden roof design. Children can become trapped in gaps between the roof structure and gable decoration.
Red Mountain Compounding Pharmacy is recalling TEST CYP 25MG/ML in Ethyl Oleate because FDA inspection raised concerns about sterility assurance. Approximately 494 patients in seven states received prescriptions for this drug.
W.L. Gore is recalling 138 units of GORE Cardioform Septal Occluder devices labeled with a 3-year expiration date instead of the actual 2-year shelf life.
Red Mountain Compounding Pharmacy is recalling Acetylcysteine 2% Ophthalmic Solution due to lack of assurance of sterility. The FDA identified concerns during an inspection of the manufacturing facility.
Red Mountain Compounding Pharmacy is recalling Vitamin B Complex Injectable Solution (HP) due to lack of assurance of sterility raised during FDA inspection. Approximately 494 patients across seven states received affected prescriptions.
Red Mountain Compounding Pharmacy is recalling MIC 25/50/50MG/ML MDV injectable medication due to lack of assurance of sterility following an FDA inspection. Approximately 494 patients in seven states received prescriptions for the affected product.
Siemens is recalling Advia Chemistry Urinary/Cerebrospinal Fluid Protein reagent due to potential reagent carryover that may cause falsely depressed Hemoglobin A1c results, which could affect clinical decisions about patient treatment.
Red Mountain Compounding Pharmacy is recalling Benzalkonium Chloride 0.013% Solution due to lack of assurance of sterility identified during an FDA inspection. Approximately 494 patients in seven states received prescriptions for this product.
Volkswagen is recalling 2022 Tiguan vehicles with a loose brake pipe nut near the right-front wheel well. The loose nut could cause brake fluid to leak, reducing braking power and increasing crash risk.
Siemens Healthcare is recalling Atellica CH Urinary/Cerebrospinal Fluid Protein reagent due to potential carryover causing falsely depressed Hemoglobin A1c results that may affect clinical decision-making.
Volkswagen is recalling one 2021 ID.4 vehicle with a defective steering gear. A missing or incorrectly assembled drive bushing may cause loss of steering control and increase crash risk.
W L Gore recalled 846 GORE CARDIOFORM Septal Occluder units labeled with a 3-year expiration instead of the correct 2-year expiration.
Olympus recalls ASC PneumoLiner surgical devices due to incorrect orientation of the containment bag that deploys upside down. This increases the risk of trapping bowel tissue during gynecologic laparoscopic surgery.
Red Mountain Compounding Pharmacy is recalling Dexpanthenol 250mg/mL injection solution due to FDA findings that sterility assurance cannot be confirmed. The product was distributed to approximately 494 patients across seven states.