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.
Polaris is recalling approximately 9,900 Sportsman 570 ATVs because the air intake duct can contact the fuel rail, causing a fuel leak and fire hazard.
GLOPO is recalling Joyrider three-wheeled scooters because the front wheels can detach while riding, posing a fall hazard to children.
Oscor, Inc. is recalling eight Adelante Breezeway sheaths because a fragment of the inner liner detached during insertion, posing a risk of device failure.
Medtronic is recalling 315 units of the PowerCross .018 OTW PTA Dilatation Catheter due to a manufacturing defect causing the balloon to fail to inflate or deflate properly.
Oscor, Inc. is recalling 45 units of Medtronic Arrive Braided Transseptal Sheaths because a fragment of the inner liner detached during insertion.
Hummingbird Wholesale is recalling Ariels OM Grown Granola because it was contaminated with wheat seed. The product was distributed in California, Oregon, and Washington.
Oscor, Inc. is recalling Medtronic Arrive Braided Transseptal Sheaths because a fragment of the inner liner may come out during insertion.
Exactech, Inc. is recalling 2,278 Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kits because disengaged screw heads may not be retained in the screwdriver.
Crescent Vending Co. Inc. is recalling 6 oz. vegetable and dip products due to undeclared soy and milk allergens.
Wakefern Food Corp. is recalling specific packs of Gourmet Oatmeal Raisin Cookies because they may contain metal pieces.
Oscor, Inc. is recalling 55 units of Medtronic Arrive Braided Transseptal Sheaths because a fragment of the inner liner detached during insertion.
Crescent Vending Co. Inc. is recalling 20 chicken salad sandwiches on Kaiser rolls in Pennsylvania due to undeclared wheat, soy, and milk allergens.
Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout due to undeclared soy.
Brownwood Farms is recalling Cherry BBQ Sauce because it contains soy ingredients that are not declared on the label.
Linnane & Co is recalling frozen shrimp cakes because the packaging failed to declare soy, sulfites, Yellow #5, MSG, and an unpermitted food color.
Wakefern Food Corp. is recalling 24-count Double Chocolate Cookies because they may contain metal pieces. The product was distributed in six states.
Ansell Healthcare Products is recalling 15 cases of Gammex Non-Latex Surgical Gloves because they incorrectly contained natural rubber latex gloves.
Chrysler is recalling one 2017 RAM ProMaster City because its side curtain air bags may not inflate properly in a crash.
Oscor, Inc. is recalling 110 units of the Adelante Breezeway sheath because a fragment of the inner liner detached during insertion.
Real Fudge is recalling Peanut Butter Fudge because it contains undeclared Blue #1, a food dye not listed on the label.
Maserati is recalling 2017 Levante S vehicles because engine software may cause the transmission to shift to neutral or the engine to shut down at low speeds.
Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout due to undeclared soy. Hot jerky salmon and jerky salmon are excluded.
Crescent Vending Co. Inc. is recalling 26 raisin bagel sandwiches with cream cheese due to undeclared wheat, soy, and milk allergens.
Oscor, Inc. is recalling 30 units of the Adelante Breezeway sheath because a fragment of the inner liner detached during insertion.
Oscor, Inc. is recalling 61 units of the Adelante Breezeway sheath because a fragment of the inner liner detached during insertion. The product was distributed in the US and internationally.