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.
AP Racing is recalling 16.9oz bottles of Super 600 Brake Fluid because the labels are missing required DOT information regarding track-only use and fluid type.
Daimler Vans USA is recalling 2017 Mercedes-Benz and Freightliner Sprinter 3500 vehicles because the Crosswind Assist system may fail to activate automatic braking in strong crosswinds, increasing crash risk.
Pier 1 Imports is recalling decorative glass pumpkins because the wooden stems can detach, causing the glass to break and cut consumers.
Todd Snyder is recalling approximately 2,100 men's sweatshirts in the U.S. because they fail to meet federal flammability standards, posing a burn risk to users.
Hunter Fan Company is recalling Contempo ceiling fans because incorrect installation instructions may cause the light globe to fall, posing an impact injury hazard.
FLAVORx Inc. is recalling Sweetening Enhancer AQ bottles due to microbial growth detected during stability testing. The product is used as a pharmacy compounding material.
Won Industry Co. is recalling three unapproved Compressible Limb Therapy Systems because they have incorrect air compression level setups. The devices were distributed in Maryland, Texas, and Mexico.
H. A. R. Maspeth Corp. is recalling Woldong World's Best Kimchi due to undeclared sesame seeds. The product was distributed in nine states.
Virginia Diner Inc. is recalling 60 cans of Plow & Hearth Chocolate Covered Cashews because peanuts were found in the product, posing a risk to individuals with peanut allergies.
Plow and Hearth is recalling 1,332 units of 10-ounce Cashew Towers because the product contains salted peanuts instead of cashews, posing an undeclared allergen risk.
Detroit City Nut, LLC is voluntarily recalling Dark Chocolate Peanuts, Almonds, and Raisins due to undeclared milk.
New Century Snacks LLC is recalling Raley's Purely Made Dry Roasted Unsalted Peanuts because some packages may be mislabeled as macadamia nuts.
Leclerc Foods USA is recalling Fit & Active Chocolatey Chip Protein Meal Bars because flexible pieces of yellow plastic were found in the product.
Becton Dickinson is recalling Trypticase Soy Agar with 5% Sheep Blood plates because they are contaminated with Listeria monocytogenes. The affected lots are distributed worldwide.
Biosense Webster is recalling 185 SMARTABLATE RF System Generators because they may inadvertently deliver RF energy if the foot pedal is placed near Stereotaxis magnets.
Becton Dickinson is recalling 2,598,000 BD Precision Glide Needles due to hub damage that can cause breakage or leakage during use.
Detroit City Nut, LLC is voluntarily recalling Dark Chocolate Almonds, Raisins, and Peanuts due to undeclared milk.
Pro-Med Instruments is recalling DORO Sterile Disposable Skull Pins because two instances of pin tip breakage were reported during surgery.
FLAVORx Inc. is recalling specific lots of Sweetening Enhancer used in pharmacy compounding due to microbial growth detected in stability testing.
Roche Diabetes Care is recalling the Accu-Chek Connect app because a bug in the Bolus Advisor feature may prevent correction bolus advice from being available for recent glucose readings.
Dominguez Family Enterprises is recalling Juanita's Brand OJOS Mexican Pastry due to undeclared coconut. The product was distributed in Oregon and Washington.
Meijer Distribution is recalling specific lots of cashews that contain undeclared mixed nuts instead of chocolate covered cashews.
GE Medical Systems is recalling CARESCAPE Patient Data Module software because it fails to generate visual or audible alarms for impedance respiration apnea events.
ICU Medical Inc is recalling MedNet 6.1 and 6.21 software because it may alter piggyback medication settings without user notice.
Detroit City Nut is voluntarily recalling Dark Chocolate Almonds due to undeclared milk, a common allergen, as part of a supplier recall.