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 2022 RAV4, RAV4 Hybrid, and RAV4 Prime vehicles because a front passenger seat occupant detection sensor may fail to properly detect occupants. This could cause improper air bag deployment during a crash, increasing injury risk.
Jaguar is recalling 2022 XF, F-Type, and F-Pace vehicles because the driver and front passenger seat belt pretensioners may be damaged, causing improper restraint during a crash.
The Hammock Source is recalling about 32,500 Key West Knock Down Hammock Stands because the weld attaching the stand to the base can break, posing a fall hazard. Nine reports of stands breaking have been received, including two reports of scrapes and bruises.
Nissan recalls 2022 Pathfinder rental vehicles where a software defect can disable the rearview camera, increasing crash risk. Affected customers will receive a free software update via dealer or over-the-air update.
Subaru recalls 2015-2021 WRX vehicles; backup light switch may corrode and fail, disabling backup lights and rearview camera in reverse, reducing visibility and increasing crash risk.
Jaguar is recalling 2021-2022 F-PACE vehicles because incorrect tail lights may cause rear turn signals to fail, increasing crash risk.
Monti Kids is recalling about 1,500 Toy Box with Bins units sold online from July 2021 through February 2022 because a small dowel can become exposed and detach, posing a choking hazard to young children.
Tesla is recalling certain 2022 Model S vehicles because the front bumper carrier structure may alter crash detection, causing the front passenger airbag to deploy incorrectly during low speed crashes. This increases the risk of passenger injury.
Toyota is recalling certain 2022-2023 Tacoma vehicles due to insufficient welds in the upper child seat anchors. These defects may prevent proper anchoring of child seats, increasing the risk of injury during crashes or sudden stops.
Vichy Laboratoires is recalling LiftActiv Peptide-C Anti-Aging Ampoules because the glass vials can break when opened, causing cuts to fingers and hands. The manufacturer has received 35 injury reports, including one requiring stitches.
Aqualung i330R SCUBA diving computers can fail to adjust for user altitude and display incorrect dive-time calculations above 3,000 feet, creating risks of decompression sickness and drowning.
Tailor Made Compounding is recalling 180 vials of BCAA (branched-chain amino acid) injections nationwide due to inability to assure the product maintained sterility. Affected batches expire between April and June 2022.
Volkswagen is recalling certain 2019-2021 Audi Q8 and 2020-2021 Audi Q7 vehicles due to a fuel pump component that may break, causing the pump to fail. A failed fuel pump can stall the engine, increasing crash risk.
Tailor Made Compounding is recalling Biotin 5mg/mL injections distributed nationwide and in Puerto Rico because the manufacturer cannot assure the products were sterilized according to FDA standards.
Tailor Made Compounding is recalling ascorbic acid injectable vials due to lack of sterility assurance. The affected vials were distributed nationwide and in Puerto Rico.
Testosterone propionate injectable vials are being recalled due to lack of assurance of sterility. The recall affects product distributed nationwide in the USA and Puerto Rico.
Waldemar Link is recalling Endo Model Modular Femur and Tibia orthopedic prostheses because the blind screws on the tibial component cannot be loosened during surgery, potentially prolonging procedures.
Tailor Made Compounding is recalling 414 vials of Testosterone Enanthate 200mg/ml (5 mL and 10 mL) due to lack of assurance of sterility. The product was distributed nationwide in the USA and Puerto Rico.
Tailor Made Compounding is recalling 232 vials of Methionine/Inositol/Choline B12 injectable across the U.S. and Puerto Rico due to lack of assurance of sterility. Patients who received this medication should contact their healthcare provider.
Jubilant Draximage Inc. is recalling Draximage MAA, an injectable diagnostic drug kit, due to failed endotoxin testing. The recall affects 519 cartons distributed nationwide (Lot 1H005, expiration November 30, 2023).
TMC Acquisition LLC is recalling specific batches of Hydroxocobalamin Preservative Free injectable due to lack of sterility assurance. The affected vials were distributed nationwide in the USA and Puerto Rico.
Tailor Made Compounding recalls 41 vials of Testosterone Cypionate/Anastrozole due to lack of assured sterility. FDA Class II recall affects products distributed nationwide.
Fresenius Medical Care is recalling 656 cases of NATURALYTE Liquid Acid dialysate nationwide (lot 22CTAC106) because alternate bottle caps are not qualified for use, potentially compromising product integrity.
Draeger Medical is recalling neonatal transport systems because an oxygen supply component is not rated for the system's working pressure. This affects 38 units distributed internationally but not in the United States.
Medtronic MiniMed is recalling approximately 575 MiniMed 720G Insulin Pumps due to battery cap deterioration that may result in power loss and device malfunction.