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.
Pierce is recalling 2010-2022 fire trucks because stokes basket brackets may be insufficiently welded, posing an injury risk if they fail.
Brother is recalling Meic AC power adapters sold with AirSure DF-2 tabletop air purifiers because the adapter casing can break during plugging or unplugging, exposing metal prongs that pose electrical shock and electrocution hazards.
Radio Flyer is recalling the Tesla Cyberquad for Kids (Model 914) because it violates federal safety standards for youth ATVs and lacks a required CPSC-approved action plan. One incident involving a tip-over has been reported.
Chrysler and Dodge are recalling certain 2022 models because the tire pressure monitoring system sensor battery may fail prematurely, potentially increasing the risk of tire failure and crashes.
Bike USA is recalling about 3,400 Punisher Adult Cycling Helmets sold online from July 2020 through December 2021. The helmets do not meet safety standards for impact protection and can fail to protect the wearer in a crash.
Siemens N Antiserum to Human IgG reagent batches are not meeting performance standards for high-dose immunoassay testing. The issue affects 10,201 packs distributed nationwide and may result in inaccurate diagnostic test results.
Flathau's Fine Foods is recalling Cheese Straws Delta Bred products due to undeclared wheat and milk allergens. 433 units were distributed across 12 states. Consumers with allergies should stop consuming and discard affected products.
Medline recalls CENTURION SnagFree Chest Tube insertion trays because a silk suture component was sterilized twice instead of once, potentially compromising its integrity. The affected lot contains 18 kits distributed in California and Texas.
Abbott is recalling MitraClip and TriClip Clip Delivery Systems due to clip locking malfunctions. Failed procedures may result in mitral regurgitation recurrence, device embolization, or tissue injury.
Abbott Vascular is recalling MitraClip Clip Delivery System devices due to observed increases in clip locking malfunctions that can lead to recurrence of mitral regurgitation, device embolization, or tissue injury.
Synthes surgical implant kits are being recalled because they contain an incorrect size drill guide that cannot properly prepare the bone for the implant, creating a risk of bone damage during surgery.
Lyons Magnus LLC is recalling Lyons Ready Care Thickened Orange Juice 46 fl oz cartons due to indication of product spoilage. Specific lot numbers distributed nationwide are affected.
Lyons Magnus LLC is recalling Lyons Ready Care Thickened Apple Honey Nectar due to indications of product spoilage. The nationwide recall affects 645 cases with specific lot numbers and best-by dates in March 2023.
Synthes is recalling SPEED 9X10X10mm surgical implant kits nationwide due to an incorrect-size drill guide that will not properly prepare bone for the implant, creating potential for bone damage.
Medicina Uk Ltd is recalling Medicina Reusable Oral syringes because the plunger was manufactured with polyethylene instead of the required polypropylene material. The 11,100 affected syringes do not meet raw material specifications.
Medicina UK Ltd is recalling Reusable Oral Syringes because plungers were manufactured from unapproved polyethylene instead of the specified polypropylene material.
Karlsburger Kitchens beef gravy mix is recalled for containing undeclared gluten despite its gluten-free label. The product poses a risk to consumers with celiac disease or gluten sensitivity.
Flowers Foods is recalling Tastykake Glazed Caramel Apple Pie because some packages contain undeclared soy lecithin, a major food allergen. Consumers with soy allergies should not consume this product.
ARROW INTERNATIONAL Inc. is recalling an ARROW Pressure Injectable Arrowgard Blue Advance Midline Catheter Kit due to mislabeling. The package labels incorrectly specify a double-lumen 5.5 French catheter, but the kit contains a single-lumen 4.5 French catheter.
Lyons Magnus is recalling Imperial Thickened Cranberry Cocktail Nectar due to indication of product spoilage. Approximately 2094 cases were distributed nationwide.
Karlsburger Kitchens NSLP 140 Turkey Gravy Mix labeled as gluten-free contains undeclared gluten. The product was distributed in Kansas, Minnesota, Nebraska, and Wisconsin.
B. Braun is recalling CARESITE SMALLBORE EXT SET T-PORT 5 IN. devices due to potential bonded joint failure that could cause leakage or detachment during use. The malfunction may result in delayed therapy, bloodstream infection risk, and exposure to hazardous medications.
Market Pantry White Fudge Animal Cookies sold at Target may contain metal fragments. D. F. Stauffer Biscuit Co is recalling 883 cases distributed nationwide.
Seeking Health LLC is recalling Optimal Multivitamin Chewable Dietary Supplement tablets because lab testing found higher copper levels than stated on the label.
Lyons Magnus is recalling Imperial Thickened Cranberry Cocktail Honey due to indication of product spoilage. Consumers who have purchased affected cases should stop using the product.