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.

2276–2300 of 52932

  • HighFDA (Devices)·Z-1105-2026·2026-01-28

    RayStation 12A treatment planning recalled over dose that fails to invalidate

    RaySearch Laboratories is recalling RayStation/RayPlan models 13.0.0.1547, 13.1.0.144 and 13.1.1.89 because calculated radiation dose is not invalidated as intended for certain regions of interest.

    Product
    Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 13.0.0.1547, 13.1.0.144, 13.1.1.89 Software Version: RayStation 12A, RayStation 12A SP1, RayStation 12A SP2 Product Description: Radiation Therapy Treatment Planning System Component: No
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1104-2026·2026-01-28

    RayStation 11B treatment planning recalled over dose that fails to invalidate

    RaySearch Laboratories is recalling RayStation/RayPlan models 12.0.0, 12.1.0, 12.0.3, 12.0.4 and 12.3.0 because calculated radiation dose is not invalidated as intended for certain regions of interest.

    Product
    RayStation/RayPlan. Model/Catalog Numbers: 12.0.0, 12.1.0, 12.0.3, 12.0.4, 12.3.0. Software Version: RayStation 11B, RayStation 11B SP1, RayStation 11B SP2, RayStation 11B SP3, RayStation 11B SPT1. Radiation Therapy Treatment Planning System
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1107-2026·2026-01-28

    Blood transfusion filters recalled over unconfirmed sterility assurance before release

    GVS TM is recalling 2,720 SQ40S Blood Transfusion Filters from one lot because they were released for distribution before the required quality control release process was completed.

    Product
    Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 10.1.1 Software Version: RayStation 10B SP1 Product Description: Radiation Therapy Treatment Planning System Component: No
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1112-2026·2026-01-28

    PET scanners recalled over a streaking artifact in clinical images

    GE HealthCare is recalling 364 Omni Legend PET systems because an intermittent issue can produce a streaking artifact in PET clinical scan images.

    Product
    GE Healthcare Omni Legend, sold under the following names: OMNI Legend 16, Omni Legend 21, OMNI Legend 32, Omni Legend PET Gantry 16cm - MEA, Omni Legend PET Gantry 16cm Haifa LM, Omni Legend PET Gantry 16cm Mobile, Omni Legend PET Gantry 21cm - BJ for Global, Omni Legend PET
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V045000·2026-01-26

    Keystone Recalls 2026 Coleman Travel Trailers Due to Bed Bracket Defect

    Keystone is recalling 2026 Coleman travel trailers because bed brackets may not be secured to a stud, causing the bed to fall unexpectedly and increasing injury risk.

    Product
    KEYSTONE — KEYSTONE COLEMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V046000·2026-01-26

    Kia vehicles recalled for instrument panel display software failure

    Kia is recalling multiple 2025–2026 models due to a software error that may cause the instrument panel display to fail, potentially hiding critical safety information like the speedometer and warning lights.

    Product
    KIA — KIA SPORTAGE PHEV, SORENTO PHEV, SPORTAGE HYBRID, SPORTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V047000·2026-01-26

    Hyundai vehicles instrument panel display software error recall

    Hyundai is recalling certain 2025–2026 Tucson Hybrid, Tucson PHEV, and other 2026 models due to a software error that may cause the instrument panel display to fail, potentially hiding critical safety information like the speedometer and warning lights.

    Product
    HYUNDAI — HYUNDAI PALISADE HYBRID, PALISADE, KONA, IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V043000·2026-01-23

    2026 Brinkley RV Model Z Trailers Recalled for Fire Risk

    Brinkley RV is recalling certain 2026 Model Z trailers because shore power inlet lugs may be improperly tightened, causing wires to loosen, overheat, and create a fire hazard.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V038000·2026-01-23

    Toyota Tundra rearview camera image may not display when reversing

    Toyota is recalling certain 2024-2025 Tundra and Tundra Hybrid vehicles with a Panoramic View Monitor because the rearview camera image may not display when the vehicle is placed in reverse.

    Product
    TOYOTA — TOYOTA TUNDRA, TUNDRA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V039000·2026-01-23

    Forest River Recalls 2026 Trailers Due to Wiring Fire Risk

    Forest River is recalling 2026 Cherokee, Campsite Reserve, and Cascade trailers because incorrect wiring lacks over-current protection, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER CASCADE, CAMPSITE RESERVE, CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26208·2026-01-22

    Magnetic stick figure toy sets recalled over loose ingestible magnets

    About 1,600 Vndueey Magnetic Men toy sets are being recalled because they contain magnets that can be swallowed by children. CPSC reports no injuries or incidents.

    Product
    Vndueey Magnetic Men Toy Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26203·2026-01-22

    Treadmills recalled over power cords that can loosen from the socket

    About 47,000 Matrix and Vision treadmills are being recalled because the power cord can become loose from the power socket, posing a fire hazard.

    Product
    Matrix Retail T30, TF30, T50, TF50, and T75 treadmills, Vision T9800, TF20, T40, and T80 treadmills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26207·2026-01-22

    Fidget magnet ball toys recalled over loose high-powered magnets

    About 9,300 Based Online Fidget Magnet Ball Toy Sets are being recalled because they contain magnets that can be swallowed by children. CPSC reports no injuries or incidents.

    Product
    Based Online Fidget Magnet Ball Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26202·2026-01-22

    Folding rocker chairs recalled over legs that can break

    About 35,300 Magellan Odyssey Rocker Chairs sold by Academy Sports + Outdoors are being recalled because the chairs' legs can break.

    Product
    Magellan Odyssey Rocker Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26206·2026-01-22

    Torch lighters recalled over a lack of child-resistant mechanisms

    About 7,500 Topkay Torch Lighters are being recalled because they do not have the child-resistant mechanisms required by the mandatory standard for multipurpose lighters.

    Product
    Topkay Torch Lighters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0262-2026·2026-01-21

    Aleve recalled over insanitary conditions at a distribution center

    Gold Star Distribution is recalling Aleve over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.

    Product
    Aleve 1's, 60 CT
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1044-2026·2026-01-21

    SMV DSX New Line systems recalled over a potential detector fall

    GE HealthCare is recalling 7 units of the SMV DSX New Line nuclear medicine system, because systems moved without adequate detector support may suffer a detector fall.

    Product
    SMV DSX New Line, System, Tomography, Computed, Emission
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1084-2026·2026-01-21

    Lucky Ice mouthwash recalled over insanitary conditions at a distribution center

    Gold Star Distribution is recalling Lucky Ice Cool Mouthwash over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.

    Product
    Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is intended for the qualitative detection in plasma or serum of the anti-heparin-platelet factor 4 (PF4) antibodies generated during the type II heparin-induced thrombocytopenia (HIT type II) by ELISA.
    Category
    Drug
    Distribution
    Distributed nationwide