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.
McClure's Pies & Salads, Inc. is recalling Pecan Pies because the ingredient list says 'flour' but does not specify wheat, a major allergen.
McClure's, Inc. is recalling Egg Custard Pies because the ingredient list says 'flour' without specifying wheat, posing a risk to consumers with wheat allergies.
McClure's Pies & Salads is recalling Chocolate Shoo Fly Pies because the ingredient list says 'flour' but does not specify wheat, a major allergen.
ConMed Linvatec is recalling 57 Xenon Universal Light Source units used for endoscopic illumination due to a Class II recall.
McClure's Pies & Salads, Inc. is recalling 156 Lemon Glazed Cakes because the ingredient statement does not list Yellow #5, an undeclared allergen.
Abbott Vascular is recalling Armada 35 and Armada 35 LL PTA Catheters because some devices may have difficulty inflating or deflating.
McClure's Pies & Salads, Inc. is recalling Black Walnut Cakes because the ingredient list says 'flour' instead of 'wheat flour', posing a risk to people with wheat allergies.
McClure's Pies & Salads, Inc. is recalling Apple Dumplings because the ingredient list says 'flour' but does not specify wheat, posing a risk to people with wheat allergies.
Toshiba American Medical Systems is recalling three Aquilion One CT systems because the SureStart function may fail, leading to abnormal cerebral blood flow analysis results.
McClure's Pies & Salads is recalling Coconut Cream Pies because the ingredient list says 'flour' without specifying wheat, posing a risk to people with wheat allergies.
Yakima is recalling specific rooftop rack systems for 2012-2013 Ford Focus vehicles because they may slide off when loaded, posing a hazard to others.
Aston Martin is recalling 2010-2012 V12 Vantage Coupes because the tire pressure warning light may not illuminate until pressure is significantly low.
Haier America is recalling 42-inch LED TVs because the stand's neck support can break, causing the TV to tip over. No injuries have been reported.
Kubota is recalling about 970 RTV500 off-road utility vehicles because carbon monoxide can accumulate in the cab, posing a poisoning risk.
Cabot is recalling Wood Cleaner and Wood Brightener products with spray pumps because the seal can fail, causing chemical leaks that may burn skin or eyes.
Starcraft RV is recalling 2012 and 2013 AR-One travel trailers because inaccurate load capacity labels may lead to incorrect tire replacements, increasing crash risk.
ADS is recalling Cyclone Swing Seats because the plastic can break during use, posing a fall hazard to children. No injuries have been reported.
Dillon Importing is recalling Captain Cutlass Toy Pirate Pistols because the surface paint contains excessive lead, violating federal standards. No injuries have been reported.
Atomic Aquatics is recalling Cobalt dive computers because the lens can blow off, causing impact injuries or gas leaks that pose a drowning risk.
Evenflo recalls specific Big Kid booster seats shipped to institutional customers without instruction manuals or registration cards, increasing crash injury risk.
San Francisco Herb & Natural Food Company is recalling Paprika Sweet Powder after inspectors found a pervasive mouse infestation in the facility.
Asahi Kasei is recalling REXEED hemodialyzers after identifying a negative trend in adverse events potentially linked to a manufacturing change.
Asahi Kasei is recalling 24 units of REXEED 15 LX hemodialyzers due to a negative trend in adverse events potentially linked to manufacturing changes.
Philips Healthcare Inc. is recalling four DigitalDiagnost Systems because the GEO Transformer does not meet international electrical safety standards.
RaySearch Laboratories issued a field notice for TomoTherapy SharePlan software due to two unexpected behaviors not clearly described in the user manual. No patient mistreatment or incidents have occurred.