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.
Twin City Foods Inc. is recalling Signature Kitchens Green Peas & Diced Carrots due to potential Listeria monocytogenes contamination.
Shippert Medical Technologies is recalling Tissu-Trans FILTRON 500 sterile pouches because a cut or hole in the packaging may compromise the product's sterility.
Philips is recalling 3,177 SureSigns VS3 monitors because a software defect prevents the device from measuring, displaying, or alarming for pulse rates above 240 beats per minute.
Volkswagen is recalling 2012-2020 Passat and 2018-2019 Atlas vehicles because a missing blocking cap allows headlight aim to be adjusted out of specification, increasing crash risk.
Dangonds Foods LLC is recalling Dangonds Arepas de Queso because the label fails to list milk as an ingredient. The issue was identified during a Florida Department of Agriculture inspection.
Philips is recalling 366 SureSigns VS4 monitors because software prevents the device from measuring or alarming for pulse rates above 240 beats per minute.
Shippert Medical Technologies is voluntarily recalling 6,553 units of Tissu-Trans FILTRON 2000 sterile, disposable, one-patient use devices due to a Class II classification.
Shippert Medical Technologies is recalling Tissu-Trans MEGA 1500 sterile pouches because a cut or hole may compromise sterility.
Philips is recalling 518 SureSigns VS3 monitors because a software defect prevents the device from measuring or alarming for pulse rates above 240 beats per minute.
Abbott is recalling ARCHITECT Estradiol Reagent Kits because patient results may be falsely elevated for individuals currently or recently treated with Mifepristone.
Stryker is recalling 3,285 Power-LOAD Cot Fastening Systems because the floor plates holding ambulance cot anchors may be broken.
R82 A/S is recalling 68 Wombat Living activity chairs (wheelchairs) in North Carolina due to reports of the plastic joint connecting the back to the seat breaking.
Philips is recalling SureSigns VS4 monitors because software prevents the device from measuring or alarming for pulse rates above 240 beats per minute.
Shippert Medical Technologies is recalling Tissu-Trans FILTRON 250 sterile filters because the pouch integrity cannot be assured without visual examination.
Union Fish Company is recalling Vega White Headless Shrimp after FDA import samples tested positive for Salmonella poly D. The product was distributed in California and Hawaii.
Arctic Cat is recalling about 1,700 Textron Havoc recreational off-highway vehicles because upper front suspension arms can fail, posing a crash hazard.
PENTAX of America Inc is recalling 4 C2 CryoBalloon Catheters because incorrect default doses and increments may be transmitted to the controller if the RFID tag is not correctly readable.
Nature Delivered Inc. is recalling Graze Dark Chocolate Cherry Tarts because the product contains almonds that are not declared on the label.
AmeriHerb International Inc is recalling 108 lbs of Blessed Thistle herb due to potential contamination with generic E. coli. The product was distributed nationwide and to Canada.
AmeriHerb International Inc is recalling 103 lbs of Lemon Balm Leaf due to potential E. coli contamination. The product was distributed nationwide and to Canada.
Philips is recalling SureSigns VS3 NBP monitors because software prevents the display and alarm for pulse rates above 240 beats per minute.
Siemens is recalling 459 Artis Q angiography systems because the floating tabletop may become blocked after a collision sensor activates.
Ducati is recalling 2018-2019 Panigale motorcycles because excessive fuel tank pressure may cause fuel to spray when opening the cap, increasing injury and fire risks.
Linora Corporation is recalling WiFiRanger DC Step-Up power converters because they may overheat, increasing the risk of a fire.
Newell Coach Corp. is recalling 2017-2020 P50 motorcoaches because a short wiper arm linkage may cause the wiper to rotate downward, reducing visibility and increasing crash risk.