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.
Whole Foods Market is recalling Southwest SooFoo Salad in Northern California due to potential E. coli O157:H7 contamination in ingredients.
Atherstone Foods Inc dba Glass Onion Catering is recalling Delish Greek Style Orzo Salad because an investigation linked the supplier to an E. coli O157:H7 outbreak.
Truitt Brothers Inc. is recalling approximately 1.77 million pounds of Kraft Velveeta Cheesy Skillets Singles Ultimate Cheeseburger Mac due to misbranding and undeclared soy allergens.
Huong Duyen Meat Products is recalling approximately 130,000 pounds of beef and pork products because they contain undeclared wheat, a known allergen.
EverGreen is recalling 2013 travel trailers because a door lock defect could jam the deadbolt, trapping occupants inside the vehicle.
RSI Home Products is recalling about 14,000 Glacier Bay bathroom medicine cabinets because the mirror or back panel can detach and fall out.
Bosch Security Systems is recalling approximately 2,000 GV4 Fire Alarm Control Panels because a specific module may prevent audible or visual alarms from sounding during a fire.
Philips Selecon is recalling four- and eight-leaf barndoors for Rama stage lights because heat can cause them to detach and fall, posing an impact injury risk.
ICU Medical is recalling specific lots of NanoClave Needlefree Connectors because a small percentage of devices may leak.
Smiths Medical ASD, Inc. is recalling 93,700 units of Hypodermic Needle-Pro Fixed Needle Insulin Syringes due to visible orange or brown particulate on the needles.
ICU Medical is recalling specific lots of NanoClave Needlefree Connectors because a small percentage of devices may leak.
ANAT, LLC is recalling IMT Wellness Legume Digest 2.0 dietary supplements due to potential chloramphenicol contamination. The product was distributed in Connecticut.
Smiths Medical is recalling 54,000 Hypodermic Needle-Pro insulin syringes due to visible orange or brown particulate on the needles.
ICU Medical is recalling specific lots of NanoClave Needlefree Connectors because a small percentage of devices may leak.
ICU Medical is recalling specific lots of NanoClave Needlefree Connectors because a small percentage of devices may leak.
The Anspach Effort, Inc. is recalling specific craniotome attachments used in a case involving a patient with Creutzfeldt-Jakob Disease.
Siemens is recalling HbA1c Flex reagent cartridges due to positive bias and frequent out-of-range flags, which may affect diabetes monitoring.
ICU Medical is recalling specific lots of NanoClave Needlefree Connectors because a small percentage of devices may leak.
ICU Medical is recalling specific lots of NanoClave Needlefree Connectors because a small percentage of the devices may leak.
ICU Medical is recalling specific lots of NanoClave Needleless Connectors because a small percentage of the devices may leak.
Ansell Sandel Medical Industries is recalling specific lots of Sandel Weighted Safety Scalpels because the blades are exposed beyond the safety shield, potentially compromising sterility and causing injury.
Smiths Medical is recalling 108,000 Hypodermic Needle-Pro insulin syringes due to visible orange or brown particulate on the needles.
ICU Medical is recalling specific lots of NanoClave Needlefree Connectors because a small percentage of devices may leak.
ICU Medical is recalling specific lots of NanoClave Needleless Connectors because a small percentage of devices may leak.
Trans American Medical is recalling 68 Spectre Wireless Footswitch/Handswitch units because they may produce uncommanded X-rays.