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.
FR Conversions is recalling 2023-2024 Ram Promaster vehicles because the seat recliner mechanism may not engage, increasing injury risk during a crash.
Forest River is recalling certain 2023–2025 Solera, Forester, and Sunseeker motorhomes because the Liquid Propane line may not be properly secured, creating a fire risk if the line becomes damaged and leaks.
Braunability is recalling 2023-2024 Chrysler Voyager wheelchair vans because the seat recliner mechanism may not engage, increasing injury risk in a crash.
Kano Laboratories is recalling Super Lube Syncopen Synthetic Penetrant, Fire Resistant Hydraulic Fluid, and Metal Protectant and Corrosion Inhibitor products in sizes of five gallons or less because the packaging is not child-resistant as required by law, posing a poisoning risk to young children.
Certain 2024 Jeep Grand Cherokees may be missing foam in the front bumper, which could prevent the front airbags from deploying during a crash. Dealers will install the foam at no cost.
Custom Truck is recalling one 2020 Ford F-550 because a wiring fault may cause electrical circuits to overheat and increase fire risk.
CHZHVAN combination smoke and carbon monoxide detectors can fail to activate and may not alert users to a fire. About 6,800 units sold online via Amazon.com from August 2023 through January 2024 are affected.
Lamborghini is recalling 2023-2024 Urus Performante and Urus S vehicles because the hood latch striker may separate, causing the hood to open or detach while driving and create a road hazard.
Mazda is recalling 2024 CX-90 vehicles because the automatic emergency braking system may falsely detect objects, causing sudden braking and increasing crash risk.
Certain 2021-2023 Volkswagen ID.4 vehicles experience a software issue causing display failures that hide the speedometer and rearview camera. Dealers will update the software at no cost.
BMW is recalling 9 2025 MINI Countryman vehicles because the armrest support bracket on the rear side door panel may be improperly secured and detach during an airbag deployment, potentially striking occupants or interfering with airbag function.
Angiodynamics recalls 455 DURAFLOW 2 hemodialysis kits for loose metal shavings that could embolize, potentially requiring surgical removal.
DURAFLOW 2 vascular access kits for hemodialysis are being recalled because some units may contain loosely affixed metal shavings that could travel through blood vessels and potentially require surgical removal.
Breckenridge Pharmaceutical is recalling Duloxetine 60 mg capsules due to elevated levels of N-nitroso-duloxetine, a manufacturing impurity above FDA limits. No illnesses have been reported.
Detty Family Barbeque LTD is recalling DB Yummers Mildly Spicy Barbeque Sauce because it was manufactured without FDA-approved processing procedures. About 7,080 bottles were distributed in Kentucky and Ohio.
Angiodynamics Inc. is recalling DURAFLOW 2 vascular catheter kits used for hemodialysis and apheresis access due to potential metal shavings that may detach and travel through the vascular system, potentially requiring surgical removal.
Philips 5000 Compact Series ultrasound systems may leave unselected transesophageal transducers powered without temperature monitoring, risking patient burns during imaging procedures.
GE Healthcare is recalling certain Allia and Discovery IGS x-ray systems due to potential adhesive failure that could cause the detector, elevator, or x-ray tube to fall. No injuries reported.
Angiodynamics has voluntarily recalled 285 units of DURAMAX STACKED TIP vascular access catheters (lots 5807195 and 5807196) used for hemodialysis. The specific reason for the recall is not disclosed in the FDA notice.
GE Healthcare recalled certain Allia IGS and related fluoroscopic x-ray systems due to potential incomplete adhesive on bolts in the gantry assembly, risking detector or tube failure.
Advagen Pharma is recalling Tramadol Hydrochloride Tablets after a pharmacy discovered baclofen tablets mixed in a bottle of tramadol. This nationwide recall affects 2,592 bottles.
Breckenridge Pharmaceutical recalls Duloxetine 30mg delayed-release capsules nationwide due to N-nitroso-duloxetine impurity exceeding FDA-recommended interim limits. The impurity was identified as a CGMP manufacturing deviation.
GE Healthcare is recalling certain x-ray systems because adhesive material may not be properly attached to bolts, which could cause components to fall during use.
RemedyRepack Inc. is recalling TraMADol HCl 50 mg tablets nationwide after a pharmacist discovered a baclofen tablet in a tramadol bottle. Taking the wrong medication poses serious health risks.
Sacramento Cookie Factory recalls Original Wine Wafer - Lemon Vanilla cookies in multiple states due to undeclared milk allergen. Consumers with milk allergies should not consume this product.