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.
American Honda is recalling about 2,200 2017 Pioneer 700 recreational off-highway vehicles because a manufacturing defect may cause the front passenger seat belt buckle to fail.
Forest River is recalling 2017 XLR ToyHauler trailers because the Federal Placard incorrectly lists rear tire pressure as 50psi instead of 80psi, which could lead to tire failure.
DGFA is recalling about 200 women's scarves sold on Amazon because they fail to meet federal flammability standards, posing a burn risk.
Springs Window Fashions is recalling motorized window coverings sold with Zeus brand lithium batteries due to fire and burn hazards.
Akron Brass Company is recalling Ultrajet firefighting nozzles because internal components may bind, limiting water output and hindering firefighting efforts.
Segway is recalling specific off-board chargers for Personal Transporters because a wire can detach and cause a shock hazard. No injuries have been reported.
Combi USA is recalling about 1,000 Shuttle Travel Systems because the car seat can disengage from the stroller frame, posing a fall hazard to infants.
Honda is recalling 2015-2016 CR-Vs that received replacement engines potentially built with wrong pistons, which may cause engine stalls and increase crash risk.
Pastry Food Products Inc. is recalling 1 lb packages of Corn Sticks with Cheese because wheat is not declared on the ingredient list.
ConAgra Foods is recalling Premium Hunt's Chili Kits due to potential Salmonella contamination in the spice packets. The recall covers 5,458 cases distributed nationwide.
Lakeside Foods is recalling Season's Choice Garden Fresh Sweet Peas because testing found Listeria monocytogenes. The product was sold at ALDI stores in eight states.
Remel Inc is recalling Blood Agar plates due to confirmed surface contamination with Listeria monocytogenes. The products were distributed nationwide and in Puerto Rico.
Armada Nutrition is recalling USN B4 Bomb Extreme Pre-Workout due to a raw material testing failure for Staphylococcus aureus that was not fully investigated.
McCain Foods USA is recalling Roundy's and Harris Teeter Southern Style Diced Hash Browns because they are contaminated with extraneous golf ball material.
Armada Nutrition is recalling Performix Crea-Bead creatine powder because a raw material initially tested positive for Staphylococcus aureus, raising concerns about potential contamination.
Savaria Concord Lifts is recalling 226 Stairfriend stair lifts due to poor quality welding on the seat post.
Pastry Food Products Inc. is recalling Trigal Corn Sticks because wheat is not declared on the ingredient list.
Supermercado Econo Inc. is recalling Econo Octopus Style in Oil because the product contains squid but is labeled as octopus.
Cardiovascular Systems Inc is recalling 595 units of ViperWire Advance guide wires because 0.018-inch products were packaged as 0.014-inch.
Armada Nutrition is recalling 39,600 kg of bulk Myprotein powder because an investigation into a failed Staphylococcus aureus test was not properly conducted.
Armada Nutrition is recalling MYPRE V2 preworkout powder because a raw material initially failed testing for Staphylococcus aureus, raising concerns about potential contamination in the finished product.
Ulrich Medical USA Inc is recalling 4,854 uNion Cervical Plate Systems because static plate screws may disassociate. The recall covers devices distributed in 20 US states.
Isomeric Pharmacy Solution, LLC is recalling 1,951 vials of Triamcinolone Diacetate injection because production processes cannot assure sterility. The FDA has classified this as a Class II recall.
Merit Medical Systems is voluntarily recalling 1 mL Medallion Syringes because of a defect in the syringe plunger tip.
CareFusion is recalling 384,923 units of the SmartSite Add-On Bag Access Device because the spike port may separate or leak, potentially interrupting medication infusion.