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.
Mennel Milling Company is recalling approximately 2.6 million pounds of PIZZA 50/50 UNMALTED flour due to potential contamination with metal, wood, gasket material, and sifter balls.
Philips Azurion 5 X-ray systems with Certeray generators may experience power loss due to a potential short circuit in the power inverter board, potentially delaying or interrupting medical procedures.
W.L. Gore's GORE VIABIL Short Wire Biliary Endoprosthesis may be mislabeled regarding drainage holes, risking extended procedures, infections, and unplanned device removal in 24 units distributed in Georgia.
Philips Azurion 7 imaging systems may experience power loss due to a potential short circuit in the power inverter, risking delays or termination of diagnostic and surgical procedures.
B. Braun Medical recalls 3,890 PERIFIX epidural trays nationwide due to filter straws with incompatible neuraxial connectors instead of standard Luer connectors.
Mennel Milling Company recalls Pizza 50/50 Unmalted flour due to potential metal, wood, gasket material, and sifter ball contamination. The affected product was distributed across KY, MI, NJ, NY, and PA.
The framegrabber card in Philips Azurion interventional X-ray systems may fail to display diagnostic images properly, potentially delaying procedures.
Country Corner Dairy is recalling Sizzling Colby Cheese due to lack of proper pasteurization. The recalled product was distributed in Maryland and Virginia.
Baxter Healthcare is recalling 13,000 bags of norepinephrine bitartrate injection due to an overwrap label incorrectly showing 4 mg/250 mL concentration, while the primary bag label correctly shows the actual 8 mg/250 mL strength.
Mennel Milling Company is recalling hard wheat flour distributed in six states due to potential contamination with metal, wood, gasket material, and sifter balls. Approximately 2.6 million pounds of product may be affected.
Country Corner Dairy white cheddar cheese from Maryland and Virginia is being recalled due to inadequate pasteurization during manufacturing. The product was distributed in various sizes in vacuum-sealed packaging.
Mennel Milling Company is recalling approximately 2.6 million pounds of ALL PURPOSE EN EZ BL flour due to potential contamination with metal, wood, gasket material, and sifter balls.
Mennel Milling Company is recalling HARD E6 1036 bulk product distributed across six states due to potential contamination with metal, wood, gasket material, and sifter balls. No illnesses have been reported.
The OPTIMIZER model CCM X11 implantable pulse generator may incorrectly detect a charging error and cease delivering cardiac therapy, potentially causing patients to experience heart failure symptoms. A total of 1,469 units are affected.
FUJIFILM Synapse CV 6 medical imaging software may incorrectly calculate left ventricle mass measurements. If used for diagnosis, this calculation error could lead to patient misdiagnosis and incorrect treatment, potentially causing long-term health consequences.
Country Corner Dairy is recalling Yellow Cheddar Cheese due to lack of proper pasteurization. The product was distributed in Maryland and Virginia and may pose a food safety risk.
Henry Schein Inc. and Glove Club HSI Gloves Inc. are recalling 1,099 vials of Adrenalin (Epinephrine) Injection because the expiration date on the repack pouch label is incorrect. The product was distributed nationwide.
Fortune cookies from New World Company are recalled for containing undeclared soy allergen. The 1 lb retail bags were distributed in California to consumers.
Mennel Milling Company recalls UNBLE ENR MALTED RM6144 FLOUR for potential foreign material contamination including metal, wood, gasket material, and sifter balls. The recall affects approximately 2.6 million pounds distributed in six states.
Bestco LLC is recalling CVS Health Cherry Cough Drops nationwide due to potential glass and silicone particulates resulting from manufacturing process deviations.
USDA FSIS issued a public health alert for Nurture Life Chicken Parm with Super Veggie Spaghetti due to an undeclared egg allergen. Consumers with egg allergies should not consume the product.
Lippert is recalling MTP 20K Surge Brake Couplers with part number 2023050981 because incorrect labels may allow the brake system to be overloaded.
Tesla is recalling certain 2013-2022 Model S, X, 3, and Y vehicles because a factory reset can mute the Pedestrian Warning System sounds, increasing crash risk for pedestrians.
Pierce Manufacturing is recalling 2023-2024 Commercial Chassis because a firmware defect in specific multiplex nodes can cause electrical circuits to overheat and potentially start a fire.
Daimler Coaches is recalling 2022-2024 Mercedes-Benz Tourrider vehicles because the roof hatch handle may break, potentially delaying emergency exits.