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.
Activforce 2 medical devices (145 units) are being recalled due to a manufacturing defect causing inaccurate force measurement, which may lead to incorrect treatment planning. Verify your device's serial number against the FDA recall list.
Cardinal Health has recalled RoyalSilk Non-Reinforced Surgical Gowns XX-large due to the potential for packaging seals to open, which could compromise product sterility. The recall affects approximately 9,990 units distributed worldwide.
Cardinal Health is recalling 270,839 units of RoyalSilk Non-Reinforced Surgical Gowns (X-large, SKU 9548) due to potential packaging seal failures that could compromise sterility.
Activbody is recalling the Activ5 smart fitness device due to manufacturing defects causing inaccurate force measurements, which may lead to incorrect treatment planning. The device was distributed nationwide.
Xstrahl Limited is recalling treatment applicators for Gulmay Medical 150 and Xstrahl 150 X-ray therapy systems. The base plate may detach from the applicator body, potentially affecting treatment positioning and delivery.
Medline Industries is recalling EVLP Convenience Pack/Kit due to a NaCl injectable component that expired in April 2020, despite the kit's label showing a later expiration date. Users may unknowingly use expired medication.
Kraft Heinz Foods Company is recalling Tang orange drink mix powder (2.2 kg) due to potential glass and metal contamination. The product was distributed nationwide and internationally.
Kraft Heinz Foods Company is recalling Country Time Original Lemonade drink mix powder due to potential contamination with glass and metal fragments.
Livia Global is recalling Livia One Organic Probiotic Nasal Spray due to contamination with Pseudomonas aeruginosa, a bacterium that can cause respiratory infection.
Kraft Heinz Foods Company is recalling Arizona Arnold Palmer Half Iced Tea & Half Lemonade drink mix powder (73 oz) because the product may contain glass and metal fragments.
Krispy Kreme is recalling DOUGHNUT Bites Original Glazed in a 5-pouch 8 oz box because the product may contain metal fragments. Consumers who have purchased the affected lot should not eat the product.
Cardinal Health is recalling SmartSleeve Poly-Reinforced Breathable Sleeve Surgical Gowns (X-Large, SKU 9041) due to potential open packaging seals that could compromise sterility. The recall affects 231,219 units distributed worldwide.
Tesla is recalling 2017-2020 Model 3 vehicles because the rearview camera cable may be damaged by the trunk lid, preventing the image from displaying and increasing crash risk.
Certain 2022 Jeep Wagoneer and Grand Wagoneer vehicles have a radio software defect that may prevent the rearview camera display from functioning, reducing rear visibility and increasing crash risk. Dealers will reprogram the radio software free of charge.
Tesla is recalling 2014-2021 Model S vehicles due to a misaligned front trunk latch assembly that may prevent the secondary hood latch from engaging. This could allow the hood to open unexpectedly during driving, obstructing the driver's view and increasing crash risk.
Cruiser RV is recalling 2021-2022 Shadow Cruiser and 2022 Twilight travel trailers because certification labels may display incorrect tire information, potentially leading to the installation of wrong tires.
Daimler Trucks North America is recalling 2022 Thomas Built Minotour School Buses because the parking brake may release while the wheelchair lift is deployed, increasing injury risk.
Clek is recalling specific Liing and Liingo infant seats because labels may bubble and detach, creating a choking hazard for children.
Jayco is recalling certain 2022 Entegra Vision motorhomes because the main chassis wiring harness may be positioned too close to the exhaust manifold, causing the wiring to melt. This can lead to vehicle stall and increased crash risk.
USDA FSIS issued a public health alert for Trader Ming's frozen wonton soup containing undeclared shrimp and pork. Consumers with allergies should not consume the product.
USDA FSIS issued a public health alert for Swiss Meat Hawaiian-style summer sausage due to possible metal contamination. Consumers are urged not to consume the product.
Forest River is recalling 2020-2022 Cardinal fifth wheels because the generator compartment may not be properly sealed, potentially allowing carbon monoxide into the vehicle. Owners should contact dealers for free inspection and repair.
Micro Bird is recalling 2013-2021 G5 transit buses because a fold-away seat may block access to the emergency exit handle, delaying evacuation.
Mercedes-Benz is recalling one 2020 CLA 250 because melted adhesive may contaminate the power steering connection, risking assist failure.
Ford is recalling certain 2021 Bronco and Ranger vehicles due to a misaligned cruise control radar module that may prevent the adaptive cruise control and emergency braking systems from functioning properly, increasing crash risk.