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.
USDA issued a public health alert for Super Asian Chicken Salad containing peanut butter recalled for potential Salmonella contamination.
Ox Bodies is recalling 2019-2021 dump bodies because insufficient rear hinge welds may cause assembly failure, increasing injury risk.
Forest River is recalling certain 2021-2022 Berkshire motorhomes with an incorrect circuit breaker installed in the electrical system. The defect can cause excessive heat and create a fire risk.
Roadtrek is recalling 2021-2022 recreational vehicles with 2-burner cooktops that may develop gas leaks from damaged valves, increasing fire risk. Owners should contact Roadtrek customer service at 1-888-762-3873 for free cooktop replacement.
Ford is recalling certain 2022 F-Series and 2023 E-Series vehicles whose Safety Certification Labels are missing tire size, rim type, and pressure values. The missing information could lead to incorrect tire selection or pressure, increasing crash risk.
Keystone RV is recalling 2022 Keystone Cougar travel trailers with swing-up table/bed bases that may have incomplete welds, causing the base to drop unexpectedly and increase injury risk.
Ford is recalling 25,032 2019-2020 Mustangs with 5.0L engines and manual transmissions because a software defect may disable the reverse camera, reverse light, and driver assist features, increasing crash risk.
Daimler Trucks is recalling 2017-2022 FCCC XC Chassis vehicles because the tire pressure monitoring system may display incorrect data, increasing crash risk.
Copper Pearl is recalling approximately 1,300 children's pajamas because they fail to meet federal flammability standards for tight-fitting sleepwear, posing a risk of burn injuries to children.
General Motors is recalling certain 2022 Chevrolet Colorado vehicles with manual passenger seats due to improperly welded front seat hooks that may separate, potentially failing to properly restrain occupants in a crash.
Oshkosh is recalling 2019-2022 S-Series 2.0 Concrete Mixers because incorrectly installed alternator cable clamps may damage cables, increasing the risk of a fire.
Honda is recalling 2020 CR-V vehicles because a fuel tank clip may detach, causing inaccurate fuel gauge readings and potential stalling.
Milwaukee Performance Helmets is recalling specific models that fail to meet federal safety standards due to potential defects in retention, protection, and labeling.
Asweets is recalling about 2,000 Wonder & Wise Activity Tables because screws on the xylophone component can become loose or detach, posing a choking hazard to young children. No injuries have been reported.
Free Birdees has recalled approximately 1,530 children's pajamas that fail to meet federal flammability standards, posing a burn injury risk to children. No injuries have been reported.
McNeilus is recalling 2020-2024 mixer trucks because missing labels may prevent operators from knowing proper mixer functions, increasing injury risk.
Lupin Pharmaceuticals is recalling GaviLyte-C bowel-preparation powder nationwide (26,910 bottles) because the product failed stability testing, potentially indicating degraded ingredients or reduced effectiveness. Patients should contact their doctor for a replacement.
Luminex Corporation is recalling 24 Verigene Processor SP units because the heater may operate outside established temperature limits, potentially producing false negative diagnostic results.
Beckman Coulter is recalling DxM 1096 MicroScan WalkAway Instruments because some units may have an incorrect AC power entry connector rated at 1 ampere instead of 10 amperes, posing a potential electrical safety risk.
Boston Scientific's EXALT Model D duodenoscope is subject to updated use instructions addressing a known risk of perforation. The FDA requires updated guidance on insertion and removal procedures.
Heartware, Inc. is recalling the HeartWare Ventricular Assist Device (HVAD) in Finland and Turkey due to translation errors in device displays and supporting documentation that could impair proper device operation.
Beckman Coulter is recalling four MicroScan WalkAway-96 Plus systems that may have been assembled with a power connector rated at 1 ampere instead of the correct 10 amperes, creating an electrical hazard risk.
Plastikon Healthcare LLC is recalling 5,400 unit doses of Milk of Magnesia USP (Lot 20041A, exp. May 2022) due to failure to properly investigate failed microbial testing during manufacturing. The product was distributed in Indiana for further distribution nationwide.
Three MicroScan WalkAway-40 medical instruments were recalled because they have an AC power connector rated at 1 ampere instead of the correct 10 ampere rating. This mismatch poses a potential electrical and fire hazard.
R & S Roberts Enterprises is recalling Milk & Dark Chocolate Caramels because soy lecithin is not declared on the label despite being present from the canola oil spray used during manufacturing. Consumers with soy allergies should not consume this product.