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.

4251–4275 of 52939

  • HighNHTSA·25V326000·2025-06-23

    Western Star battery to starter stud can short circuit

    Daimler Trucks is recalling certain 2020-2026 Western Star 49X and 2021-2026 47X vehicles because a stud connecting the battery to the starter at the frame rail may have been incorrectly installed.

    Product
    WESTERN STAR — WESTERN STAR 47X, 49X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V424000·2025-06-20

    2026 Forest River Sabre Fifth Wheel Griddle Fire Risk Recall

    Forest River is recalling 2026 Sabre fifth wheel recreational trailers because the exterior griddle may be incorrectly installed, allowing it to be stowed while still connected to LPG, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER SABRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V423000·2025-06-20

    2026 Forest River Spirit travel trailers recalled for defective safety chains

    Forest River is recalling certain 2026 Spirit travel trailers because the installed safety chains may not meet the actual Gross Vehicle Weight Rating, posing a risk of trailer separation from the tow vehicle.

    Product
    FOREST RIVER — FOREST RIVER SPIRIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-06202025-01·2025-06-20

    USDA Issues Public Health Alert for Uninspected Thompson's Meat Sauce Products

    USDA FSIS issued a public health alert for Thompson's meat sauce products produced without federal inspection. Consumers in Illinois and Indiana are urged to discard the items.

    Product
    FSIS Issues Public Health Alert for Meat Sauce Products Produced Without the Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·25V405000·2025-06-19

    Shyft Recalls 2024-2025 Utilimaster Aeromaster for Camera Display Defect

    Shyft Group is recalling 2024-2025 Utilimaster Aeromaster vehicles because the 360-degree camera monitor may not display the correct image at startup, increasing crash risk.

    Product
    UTILIMASTER — UTILIMASTER AEROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V421000·2025-06-19

    Supreme Recalls 2025 Wabash Trucks Due to Liftgate Pin Seizure Risk

    Supreme is recalling 2025 Wabash trucks because insufficient lubrication on the liftgate pin may cause it to seize, leading to liftgate failure and injury risk.

    Product
    SUPREME — SUPREME WABASH TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V410000·2025-06-18

    2026 Tesla Model Y and Model 3 Vehicles Seat Fastener Recall

    Tesla is recalling certain 2026 Model Y and Model 3 vehicles because seat back fasteners may have been improperly tightened, potentially affecting proper occupant restraint during a crash.

    Product
    TESLA — TESLA MODEL 3, MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V416000·2025-06-18

    REV Recalls 2025-2026 Fleetwood and Holiday Rambler Motorhomes for Electrical Defect

    REV is recalling 2025-2026 Fleetwood Altitude and Holiday Rambler Incline motorhomes because water intrusion may cause electrical components to fail, potentially disabling carbon monoxide or propane detectors.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER ALTITUDE, INCLINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V418000·2025-06-18

    Mazda Recalls 2025 CX-50 Hybrid for Gear Shifter Safety Issue

    Mazda is recalling 2025 CX-50 Hybrid vehicles because the gear shifter can move to Drive without pressing the brake pedal, increasing crash risk.

    Product
    MAZDA — MAZDA CX-50 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25C008000·2025-06-18

    Evenflo Recalls Titan 65 Child Seats Due to Incorrect Instruction Manuals

    Evenflo is recalling Titan 65 child seats manufactured in early 2025 that may have incorrect instruction manuals, posing a risk of improper installation.

    Product
    EQUIPMENT:OTHER:OWNERS/SERVICE/OTHER MANUAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0460-2025·2025-06-18

    Celecoxib Capsules Recalled for Foreign Tablet Contamination

    AvKARE is recalling Celecoxib 200 mg capsules because one tadalafil 5 mg tablet was found in a 500-count bottle. The contamination poses a risk of unintended drug exposure to patients.

    Product
    CELECOXIB — CELECOXIB (CELECOXIB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1971-2025·2025-06-18

    BD Texium Needle-Free Syringe Recalled for Potential Leakage at Luer Interface

    BD Texium Needle-Free Syringes (multiple sizes) may leak at the interface between the male luer component and needle-free connector, potentially causing treatment delays, medication underdosing, or exposure to hazardous drugs.

    Product
    BD Texium Needle-Free Syringe: 3 mL, REF: MY8003; 5 mL, REF: MY8005; 10 mL, REF: MY8010; 20 mL, REF: MY8020; 30 mL, REF: MY8030; 60 mL, REF: MY8060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0049-2025·2025-06-18

    Creamy Butter Sauce recalled for wood-like pieces in ingredient

    GoodSource Solutions is recalling Creamy Butter Sauce (Lot 701493) because the product was manufactured with recalled cilantro containing small wood-like pieces.

    Product
    Sauce, Creamy Butter; packaged in clear, unlabeled bulk 6-pound bags/4 bags to a case. Lot code# 701493 stamped on bag.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0017-2025·2025-06-18

    Rocky Road Ice Cream 1.5 qt with Mislabeled Tree Nut Allergen

    Unilever Manufacturing is recalling Rocky Road Ice Cream due to conflicting allergen labeling—the tub says "may contain tree nuts" while the lid declares almonds are present. Consumers with tree nut allergies may be at risk.

    Product
    Rocky Road Ice Cream packaged in a Breyer Chocolate Truffle Tub that says "may contain tree nuts" with a Breyers Rocky Road Ice Cream Lid that declares almonds as an ingredient. 1.5 qt
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0018-2025·2025-06-18

    Sysco Corporation Cucumbers Recalled for Potential Salmonella Contamination

    Sysco Corporation is recalling cucumber products sold under the Imperial Fresh, East Coast Fresh, Just Cut, Wellsley Farms, and other brands due to potential Salmonella contamination. The products were distributed to multiple states and Puerto Rico.

    Product
    3909520 2/5# IMPERIAL FRESH CUCUMBER DICED 3/8 SK-ON ALL LOT CODES 480414 2/5 # IMPERIAL FRESH FC CUCUMBER STRIPED AND SLICED ALL LOT CODES 481768 12/3 OZ IMPERIAL FRESH FC VEG VEGGIE W/HUMMUS SMALL P ALL LOT CODES 511666 2/5 # IMPERIAL FRESH FC CUCUMBER SLICED SKIN ON ALL LOT CO
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-1922-2025·2025-06-18

    Soltive SuperPulsed Laser Fibers recalled for thermal incident risk

    Olympus Corporation of the Americas is recalling Soltive SuperPulsed Laser Fibers due to potential fiber fracturing that can cause thermal incidents including smoke, sparks, burning, or unsteady flames during clinical use.

    Product
    Brand Name: Powered Laser Surgical Instrument Product Name: Soltive SuperPulsed Laser Fibers - Single Use Model/Catalog Numbers: TFL-FBX150BS, TFL-FBX200BS, TFL-FBX150S, TFL-FBX200S, TFL-FBX365S, TFL-FBX550S, TLF-FBX940S, TFL-FBX150BS-JA (Japan Only), TFL-FBX550S-JA (Japan Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1974-2025·2025-06-18

    BD TEXIUM Closed Male Luer Devices Recalled for Leaking Interface Risk

    BD TEXIUM closed male luer drug transfer devices may leak at the interface between the closed male luer component and the needle-free connector, potentially causing procedure delays, treatment interruptions, hazardous drug exposure, and medication underdosing.

    Product
    BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP, REF: 10012241; BD TEXIUM (China), REF: 10012241 CHINA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1927-2025·2025-06-18

    EPIONE Stereotactic Device Software Bug Poses Instrument Guidance Risk

    The EPIONE Model 30-0001 stereotactic device is recalled due to a software bug that may cause the robotic arm to incorrectly guide surgical instruments during CT-guided ablation procedures. Four units have been distributed in the U.S.

    Product
    EPIONE Model 30-0001 UDI-DI code: 03760305400031 The EPIONE¿ device is a user controlled, stereotactic accessory intended to assist in the planning and manual advancement of one or more instruments, as well as in verification of instrument position during Computed Tomography
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1914-2025·2025-06-18

    Stryker Gamma4 Long Nail with incorrect left-nail geometry recalled

    Stryker GmbH is recalling a specific lot of Gamma4 Right Long Nails (Catalog Number 84250320S) because they were manufactured with left-nail geometry instead of right-nail geometry, which could affect surgical fit and function.

    Product
    Long Nail, RIGHT Gamma4 10x320mm x 125, component of the Gamma4 System. Catalog Number: 84250320S.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·25341·2025-06-18

    YaFiti White 12-Drawer Dressers Recalled for Tip-Over Entrapment Hazards

    YaFiti 12-Drawer White Dressers pose serious tip-over and entrapment hazards to children if not anchored to the wall, violating federal standards. About 6,000 units sold on Amazon from September 2023 through March 2025.

    Product
    YaFiti 12-Drawer White Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25343·2025-06-18

    Polaris Ranger XP and Pro XD Kinetic ROVs Recalled for Fire Hazard

    Polaris is recalling Model Year 2023-2024 Ranger XP Kinetic and Model Year 2025 Pro XD Kinetic ROVs because water can leak through a cracked filter into the high-voltage charging harness and cause a fire. The company has received 47 reports of filter failures, including six reports of melting or fire.

    Product
    Model Year 2023-2024 Ranger XP Kinetic and Model Year 2025 Pro XD Kinetic ROVs
    Category
    Vehicle
    Distribution
    Distributed nationwide