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.
Toyota is recalling certain 2021 RAV4 Prime vehicles due to a software defect that may cause engine stall during cold-weather driving. Dealers will provide a free software update.
Paper Cape is recalling approximately 5,720 children's pajamas that fail to meet federal flammability standards for sleepwear, posing a risk of burn injuries.
General Motors is recalling certain 2023 GMC Acadia vehicles because right-front half-shaft assemblies may separate from the transmission, potentially causing loss of drive power or vehicle rollaway and increasing crash risk.
About 2,000 children's polyester robes imported by BTPEIHTD and sold on Amazon fail to meet federal flammability standards for sleepwear, posing a burn injury risk. Consumers should stop use immediately and contact the importer for a refund.
About 3,000 SGMWVB brand children's robes sold on Amazon fail to meet federal flammability standards for children's sleepwear, posing a burn injury risk. Consumers should immediately stop using them and contact the manufacturer for a refund.
Nissan is recalling 2018-2023 LEAF vehicles because the Owner's Manual has incorrect defroster operation instructions, which may reduce visibility and increase crash risk. Nissan will mail updated instructions at no charge.
The rearview camera display may not activate when a 2020 Honda Fit is started with a key due to a display power circuit design error, reducing rear visibility and increasing crash risk. Dealers will provide a free software fix.
Jaguar Land Rover is recalling certain 2019-2023 Land Rover vehicles because the engine cam carrier oil channel may become blocked, causing an oil leak that could increase fire risk. No injuries have been reported.
ChildLikeMe children's robes sold on Amazon from January through April 2022 fail to meet federal flammability standards for sleepwear, posing a burn injury risk. Consumers should stop use immediately and contact the importer for a refund.
Jaguar is recalling 2023 F-Pace vehicles because the engine cam carrier oil channel may become blocked, causing an oil leak that could increase the risk of fire. Dealers will inspect and replace the affected engine components at no cost.
Pharmacy Innovations is recalling vancomycin fortified ophthalmic solutions nationwide due to lack of sterility assurance. FDA inspection revealed insanitary conditions at the manufacturing facility.
Pharmacy Innovations is recalling Mitomycin 0.2mg/ml ophthalmic solution nationwide due to lack of sterility assurance following FDA facility inspection findings.
Pharmacy Innovations is recalling an injectable medication due to lack of sterility assurance caused by insanitary conditions at the manufacturing facility. Affected vials were distributed nationwide.
Pharmacy Innovations is recalling Acetylcysteine 10% Ophthalmic Solution nationwide due to FDA-identified insanitary manufacturing conditions that compromise product sterility. Affected batches include codes t20221011@36 and t20221108@24.
BMW is recalling 2023 2 Series Coupe vehicles because side air bag cover panels may break during deployment, increasing injury risk.
Pharmacy Innovations is recalling Buprenorphine HCL 0.9 MG/ML injectable vials nationwide due to potential sterility issues discovered during FDA facility inspection. No illnesses have been reported.
Nephron Sc Inc is recalling 387,000 vials of Asthmanefrin Racepinephrine Inhalation Solution due to short fill issues. The vials may contain insufficient solution, potentially affecting medication dosing.
Pharmacy Innovations is recalling PROGESTERONE-GS OIL 100MG/ML injectable vials distributed nationwide due to lack of sterility assurance. FDA inspection found insanitary conditions at the manufacturing facility.
Siemens myNeedle Guide software for CT imaging systems has swapped orientation labels in axial images, which could lead to misorientation during guided procedures. The software requires correction.
Pharmacy Innovations is recalling injectable methylcobalamin products in multiple strengths due to lack of sterility assurance. FDA inspection revealed insanitary facility conditions that compromise product safety.
Pharmacy Innovations is recalling Hydroxocobalamin 25MG/ML injectable vials nationwide due to insanitary facility conditions identified during FDA inspection that compromise sterility assurance.
Accord Healthcare is recalling Allopurinol 100 mg tablets due to the presence of a small piece of green plastic embedded in some tablets. The plastic poses a potential choking and ingestion hazard.
Nephron Pharmaceuticals is recalling 378 bags of 0.9% Sodium Chloride Injection nationwide due to manufacturing deviations that could create product carryover.
Wegmans Food Markets is recalling Organic Farm & Orchard Microgreens (1.75 oz) due to possible Salmonella contamination. The affected products with use-by dates December 17 and 24, 2022, were distributed across the Northeast and Mid-Atlantic.
Pharmacy Innovations is recalling magnesium chloride hexahydrate injectable (5 mL vials) distributed nationwide due to insanitary facility conditions that compromise product sterility assurance.