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.
Siemens is recalling 89 Artis zee multi units because a power supply issue may cause the X-ray generator to fail during procedures.
Cardinal Health 200, LLC is recalling Monoject Blunt Cannulas because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Cardinal Health is recalling Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Geritrex, LLC is recalling Gericare Iron Supplement Elixir due to cGMP deviations that may have resulted in microbial contamination.
Deva Holding AS is recalling Temozolomide Capsules due to manufacturing deviations that allowed possible cross-contamination with beta-lactam products.
Flowers Foods is recalling 4,793 packages of 100% Whole Wheat Hamburger Buns because they may contain small pieces of hard plastic.
Wegmans is recalling Large Ultimate Carrot Cakes because they may contain pieces of plastic. The recall affects 20,232 units sold in six states.
Randox Laboratories is recalling RX Daytona instruments due to a sensor malfunction that caused internal wire melting and scorch damage.
Cardinal Health is recalling Monoject 201 Vet Pak Hypodermic Needles due to a manufacturing defect that could compromise the product's sterility barrier.
Gulf Stream is recalling 2017 Serro Scotty S14 RBR travel trailers because the Federal Placard label displays an incorrect Gross Vehicle Weight Rating (GVWR).
Mazda is recalling 2019 Mazda3 vehicles with manual dimming mirrors because the mirror may detach, reducing rearward visibility and increasing crash risk.
Chrysler is recalling 2019 Ram 1500 vehicles because the instrument cluster may fail to illuminate driver warnings, increasing crash risk. Dealers will replace the cluster free of charge.
Spansive is recalling about 950 wireless multi-phone chargers sold in May 2019 because metallic accessories can overheat, posing a burn hazard.
Forest River is recalling 2018-2019 Starcraft Allstar, Allstar XL, and Starlite vehicles because the roof hatch external handle may break, preventing emergency egress.
H&M is recalling about 9,000 children's pajama sets because they fail to meet federal flammability standards, posing a risk of burn injuries.
Britax is recalling modified thru-bolt axles for BOB jogging strollers because the front wheel can fracture and detach, posing fall and injury hazards.
Stokke is recalling Steps Bouncers because they can detach from the Steps Chair, posing a fall hazard to infants.
Daimler Trucks North America is recalling 2019-2020 Thomas Built school buses because the roof escape hatch handle may break, hindering emergency egress.
Indiana Mills and Manufacturing Inc. is recalling certain Inflatable Head Cushions and Knee Air Bags that may fail to inflate during a crash due to improper manufacturing.
Champion Bus is recalling 2019 shuttle buses because the roof emergency hatch handle may break, preventing easy opening during an emergency.
MMDi is recalling 2019 Cummins 'G' A057P788 trailers because an improperly fastened jack handle may separate, creating a road hazard.
FCA US LLC is recalling 2018-2019 Alfa Romeo Giulia and Stelvio vehicles because the Body Control Module may display a fuel level higher than the actual amount, increasing the risk of a crash.
Olympus is recalling WM-NP2 and WM-DP2 mobile workstations because the control panel arm may cause the unit to fall over if a heavy monitor is attached.
DeRoyal is recalling 108 custom surgical packs in Oklahoma because they contain defective Cardinal Health Blunt Cannulas that could compromise sterility.
Sprouts Farmers Market is recalling 1,046 cases of Cut Leaf Spinach because testing revealed the presence of Listeria monocytogenes.