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.
Wienke LLC is recalling Wienke's Market No Sugar Added Blackberry Jam because it contains butter, which is not declared on the label.
Stevens Family Bakery & Orchard LLC is recalling 15 strawberry pies because the label failed to list butter, an undeclared milk allergen.
Wienke LLC is recalling Wienke's Market Cherry Jelly because it contains butter, which is not declared on the label.
Wienke LLC is recalling Wienke's Market Cranberry Jam because it contains butter, an ingredient not declared on the label.
Ventura Foods is recalling SunGlow European Style Butter Blend Margarine because it contains undeclared soy lecithin, a common allergen.
Stevens Family Bakery & Orchard LLC is recalling cherry pies because the label failed to list butter, which contains milk, as an ingredient.
Setra is recalling 2006-2010 S417 buses because a doorway strip may fail to prevent pinch injuries from swiveling entry doors.
Stevens Family Bakery & Orchard LLC is recalling Sugar Cream Pies because the labels failed to list butter and cream, which contain undeclared milk.
Angiodynamics, Inc. is recalling Accu2i pMTA Microwave Tissue Ablation Applicators because coolant ingress may prevent the device from delivering the desired microwave energy.
Flawless Beauty LLC is voluntarily recalling Laennec INJ placenta extract vials because they were marketed without FDA approval.
Wienke LLC is recalling Wienke's Market Apricot Jam because it contains butter, an ingredient not declared on the label.
Bard Access Systems is recalling 53,699 PowerPICC Provena Catheters due to possible leaks at the luer hub extension leg junction.
Wienke LLC is recalling Wienke's Market Rhubarb Jam because it contains butter, an ingredient not declared on the label.
Wienke LLC is recalling Wienke's Market Peach Jam because it contains butter, an ingredient not declared on the label.
Wienke LLC is recalling specific jars of No Sugar Added Seedless Strawberry Jam because they contain butter, an ingredient not listed on the label.
Palmer and Company is recalling Sea Salt Caramel Hearts because a peanut was found on the packaging. Peanuts are not listed on the label.
Wienke LLC is recalling Boysenberry Jam because it contains butter, an ingredient not listed on the label.
Wienke LLC is recalling Strawberry Rhubarb Jam because it contains butter, an ingredient not listed on the label.
Ecolab, Inc. is recalling Disposable Light Handle Covers because sterile packaging may contain gaps in the seal, potentially compromising sterility.
Angiodynamics is recalling Accu2i pMTA Microwave Tissue Ablation Applicators because coolant ingress may prevent the device from delivering microwave energy.
Wienke LLC is recalling Wienke's Market Black Raspberry Jam because it contains butter, which is not declared on the label.
Despana Brand Foods is recalling 120 jars of Don Bocarte Migs Bonito Del Norte because the product may contain elevated levels of histamine.
Philips Medical Systems is recalling BrightView X gamma cameras because collimators may drop to the floor during exchange, posing a physical hazard.
Philips is recalling 1,387 Precedence 6 imaging systems because collimators may drop to the floor during exchange, posing a risk of injury.
Altec Industries is recalling 1997-2017 aerial devices because a platform leveling yoke may fail, potentially causing occupants to fall.