The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

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.

3401–3425 of 52939

  • HighNHTSA·25V696000·2025-10-14

    Nova Bus Recalls 2019-2020 LFS Buses for Missing DOT Code on Windows

    Nova Bus is recalling 2019-2020 LFS commercial buses because driver's door windows may lack the required DOT code mark, potentially leading to incorrect glass replacement and reduced visibility.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V699000·2025-10-14

    Tesla Cybertruck front parking lights can exceed maximum brightness

    Tesla is recalling certain 2024-2026 Cybertruck vehicles running software before 2025.38.3 because the front parking lights may be too bright and exceed the maximum permitted light output.

    Product
    TESLA — TESLA CYBERTRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V695000·2025-10-13

    Ford Recalls Vehicles Due to Rearview Camera Display Issues

    Ford is recalling specific 2015-2020 models because the rearview camera may display a distorted or blank image, increasing crash risk.

    Product
    LINCOLN — LINCOLN, FORD MKT, TAURUS, MKZ, MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25T018000·2025-10-13

    Toyo Recalls Multiple Off-Road Tires Due to Tread Separation Risk

    Toyo is recalling specific off-road and all-terrain tires because production contamination may cause tread separation, increasing the risk of vehicle instability and crashes.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E067000·2025-10-10

    Ford Recalls Engine Block Heaters Due to Fire Risk

    Ford is recalling specific engine block heaters that may crack and leak coolant, causing a short circuit and increasing fire risk.

    Product
    EQUIPMENT:ELECTRICAL:ENGINE BLOCK HEATER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V691000·2025-10-10

    Ford Recalls Lincoln Nautilus and Explorer Hybrids for Pedestrian Warning Defect

    Ford is recalling 2024-2026 Lincoln Nautilus Hybrids and 2025 Explorer Hybrid police vehicles because a software error may prevent the pedestrian warning sound from playing.

    Product
    LINCOLN — LINCOLN, FORD NAUTILUS HYBRID, EXPLORER HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V684000·2025-10-10

    Brenner Tank Recalls 2026 TKQXFR Trailers Due to Valve Defect

    Brenner Tank is recalling 2026 TKQXFR tank trailers because an incorrect emergency valve may leak hazardous liquids during a crash.

    Product
    BRENNER — BRENNER TKQXFR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E066000·2025-10-10

    Ford Recalls Engine Block Heaters Due to Fire Risk

    Ford is recalling certain engine block heaters for 2023-2026 vehicles because they may overheat and cause a fire. Dealers will replace the heater element and inspect the cord.

    Product
    EQUIPMENT:ELECTRICAL:ENGINE BLOCK HEATER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V680000·2025-10-09

    Genesis Supreme Recalls One Fifth Wheel Trailer Due to Fire Risk

    Genesis Supreme RV is recalling one 2024 Supreme 28IKS fifth wheel trailer because the air conditioner soft start device may overheat and cause a fire.

    Product
    GENESIS SUPREME — GENESIS SUPREME FIFTH WHEEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V676000·2025-10-09

    Nissan and Chevrolet Vans Recalled for Fuel Pump Fuse Short Circuit Risk

    Nissan is recalling 2013-2021 NV200 and 2015-2018 Chevrolet City Express vans because a misrouted sensor harness may damage wires, causing a short circuit that could stall the engine.

    Product
    NISSAN — NISSAN, CHEVROLET NV200, NV200 TAXI, CITY EXPRESS, CHEVEROLET SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2671-2025·2025-10-08

    Antimicrobial susceptibility test cards recalled over false colistin resistance results

    bioMerieux is recalling 235,269 VITEK 2 Gram-negative AST cards containing colistin formulation cs02n because they may give false resistant results for multi-drug-resistant organisms.

    Product
    VITEK¿ 2 Gram-negative AST Test Kits (Cards) containing Colistin formulation cs02n. VITEK¿ 2 is an automated system consisting of instruments, software and reagent cards designed for the identification and antimicrobial susceptibility testing of bacteria and yeast. Export o
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0024-2026·2025-10-08

    Reprocessed 1.7mm laser atherectomy catheters recalled over sterile barrier breaches

    Northeast Scientific is recalling 616 reprocessed 1.7mm RX Turbo Elite laser atherectomy catheters because of potential breaches in the sterile barrier packaging.

    Product
    NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-156. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cle
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0023-2026·2025-10-08

    Reprocessed 1.4mm rapid exchange atherectomy catheters recalled for packaging breaches

    Northeast Scientific is recalling 1,019 reprocessed 1.4mm RX Turbo Elite laser atherectomy catheters because of potential breaches in the sterile barrier packaging.

    Product
    NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-414-159. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cle
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0017-2026·2025-10-08

    Dental implants recalled after import under non compliant temperature and storage conditions

    S.I.N. Implant System is recalling 4,367 Epikut Plus dental implants imported under temperature and storage conditions that do not comply with the instructions for use.

    Product
    IMPLANT EPIKUT PLUS MT16 3,5X10,0MM, REF: ILM 3510N; IMPLANT EPIKUT PLUS MT16 3.8X11.5MM, REF: ILM 3511N; IMPLANT EPIKUT PLUS MT16 3,5X13,0MM, REF: ILM 3513N; IMPLANT EPIKUT PLUS MT16 3,5X15,0MM, REF: ILM 3515N; IMPLANT EPIKUT PLUS MT16 3,8X10,0MM, REF: ILM 3810N; IMPLANT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0030-2026·2025-10-08

    Radiology software recalled because reports may not display fully when viewed

    Change Healthcare is recalling 12 programs running Radiology Solutions software version 14.2.2 because a software issue means radiology reports may not be fully displayed.

    Product
    Change Healthcare Radiology Solutions software version 14.2.2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0640-2025·2025-10-08

    Frozen raw shrimp recalled after product on FDA nitrofuran hold shipped

    Five cases of frozen raw easy peel shrimp are being recalled after product that was on FDA hold for high levels of nitrofuran was inadvertently distributed.

    Product
    Frozen Raw Easy Peel shrimp, IQF, 2-lb bag, 10 bags/case; Generic Brown cardboard box UPC: 021130123223
    Category
    Food
    Distribution
    1 state