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.
Paradigm Foodworks is recalling Hazelwood's Habanero Salsa due to potential peanut contamination. The product was distributed in four US states and Ontario, Canada.
New Punjab Sweets Inc. is voluntarily recalling Kaju Katri Indian snacks because they may contain undeclared cashews and artificial colors Yellow 5 and 6.
Coalescence LLC is recalling Spicy Black Bean Burger powder mix because it contains undeclared peanuts. The product was distributed to consignees in Ohio, Utah, and Michigan.
Paradigm Foodworks is recalling Soog Head Medium Pineapple Smash Salsa due to potential peanut protein contamination.
Stradis Healthcare is recalling nine Breast Packs containing Devon Light Gloves due to a manufacturer recall of the glove component.
Boba Direct, Inc. is recalling spiced chai flavored powder because it contains undeclared allergens. The product was distributed in five US states.
Paradigm Foodworks is recalling Rub with Love Ancho & Molasses Barbecue Sauce due to potential peanut protein contamination.
Boba Direct, Inc. is recalling cherry flavored powder in foil bags due to undeclared allergens. The product was distributed in five states.
Paradigm Foodworks is recalling Soog Head Mild Pineapple Smash Salsa due to potential contamination with peanut protein.
Boba Direct, Inc. is recalling 2.2 lb foil bags of avocado flavored powder because they contain undeclared allergens. The product was distributed in five states.
Spartan is recalling 2007-2015 emergency response vehicles because front wheel valve stems may rub against brake calipers, causing sudden tire deflation.
Volcano Corp is recalling 227 ComboMap Intravascular Flow and Pressure Systems due to a limitation in interoperability with the Philips Xper Flex Cardia Physiomonitoring System.
Boba Direct, Inc. is recalling lavender flavored powder due to undeclared allergens. The product was distributed in five US states.
Boba Direct, Inc. is recalling cafe latte flavored powder for containing undeclared allergens. The product was distributed in five states.
Avon is recalling approximately 27,000 nut choppers because the grinding mechanism's tines can break and fall into food, posing a risk of injury.
Boba Direct, Inc. is recalling watermelon flavored powder due to undeclared allergens. The product was distributed in five US states.
Kia is recalling 2016 Sorento vehicles because the front passenger seat belt buckle may prevent fastening, increasing injury risk in a crash.
Starcraft is recalling 800 commercial buses from 2002-2007 because they may exceed their weight rating when loaded, risking poor handling or tire failure.
Continental is recalling specific ContiProContact tires due to a risk of tread separation, which could lead to sudden air loss and a vehicle crash.
Hearth & Home Technologies is recalling about 2,000 Quadra-Fire Mt. Vernon E2 pellet stoves and inserts because fuel backup can cause glass to break, posing a laceration hazard.
Epoca International is recalling about 113,000 glass whistling kettles because the bottom can break when heated, posing laceration and burn risks.
Öhlins USA is recalling about 50 RXF 48 front forks for motocross bikes because they can break or detach, posing a crash hazard.
Black Diamond is recalling JetForce avalanche airbag packs because the motor may fail to deploy, increasing injury risk.
FDA Class II recall of Palindrome SI Chronic Catheter Sport Packs by Covidien LLC due to potential failure to meet antimicrobial specifications.
Covidien LLC is recalling Palindrome Precision SI Chronic Catheter Kits because they may not meet antimicrobial specifications. The recall affects 72,363 units in the US and 24,631 units internationally.