The Recall Desk

State

Ohio product recalls

73,219 recalls have nationwide distribution and so reach Ohio. 11,755 additional recalls listed Ohio specifically in their distribution scope.

What the numbers show

Total
11,755
Critical
2,117
Severe
2,426
Most recent
2026-09-30

Of the 11,755 recalls naming Ohio we have scored against our rubric, 2,117 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,426 (21%) are Severe.

These figures cover only the 11,755 recalls whose distribution notice names Ohio specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15726–15750 of 84974

  • HighNHTSA·23V663000·2023-09-29

    Winnebago Revel motorhomes electrical cable fire risk recall

    Winnebago is recalling certain 2020–2024 Revel motorhomes because cables near the lithium batteries may contact battery hold-down brackets, damaging the cables and causing a short circuit that increases fire risk.

    Product
    WINNEBAGO — WINNEBAGO REVEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V656000·2023-09-28

    Autocar Recalls Xpeditor and Legend Vehicles for Steering Defect

    Autocar is recalling 2022-2023 Xpeditor and 2023 Legend vehicles because a steering column bolt may not be secured, risking sudden loss of steering.

    Product
    AUTOCAR — AUTOCAR XPEDITOR, LEGEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V655000·2023-09-28

    Diamond C Trailers Recall 2023-2024 Models Due to Winch Failure

    Diamond C is recalling 2023-2024 FMAX, SDX, and PX trailers because the spare tire winch may loosen or fail, increasing crash risk.

    Product
    DIAMOND C TRAILERS — DIAMOND C TRAILERS PX, FMAX, SDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23297·2023-09-28

    Solaray Liposomal Multivitamins Recalled for Non-Child-Resistant Packaging

    Nutraceutical Corporation is recalling approximately 85,300 bottles of Solaray Liposomal Multivitamins because the packaging does not meet child-resistant requirements under the Poison Prevention Packaging Act, creating a poisoning risk for young children.

    Product
    Solaray Liposomal Multivitamins
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V657000·2023-09-28

    2023 Nissan Ariya Inverter Software May Cause Loss of Drive Power

    Nissan is recalling certain 2023 Ariya vehicles due to a potential inverter software defect that may cause an unexpected loss of drive power. The loss of drive power increases the risk of a crash.

    Product
    NISSAN — NISSAN ARIYA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23796·2023-09-28

    Polaris, Gravely, and Bobcat Utility Vehicles Seat Belt Bracket Defect

    About 280 Polaris Ranger, Pro XD, Gravely ATLAS, and Bobcat utility vehicles have defective passenger-side seat belt brackets that may separate from the frame, creating an injury risk. Consumers should stop using the vehicles and contact their dealer for repair.

    Product
    Model Year 2023 Polaris RANGER XP 1000 / XP 1000 Crew and RANGER 1000 / 1000 Crew, Model Year 2024 Polaris Pro XD Full-Size Diesel Crew, Model Year 2024 Gravely ATLAS JSV-3400, and Model Year 2024 Bobcat UV34XL Gas
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E071000·2023-09-28

    Firefly Recalls Multiplex HC Relay Cards Due to Fire Risk

    Firefly Integrations is recalling Multiplex HC Relay Cards because damaged relays may cause electrical short circuits, increasing the risk of a fire.

    Product
    EQUIPMENT:ELECTRICAL recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V654000·2023-09-28

    2024 RAM 2500 Rearview Camera Display Software Malfunction Recall

    Chrysler recalls 2024 RAM 2500 vehicles due to radio software that may prevent the rearview camera from displaying. Loss of rearview visibility increases crash risk.

    Product
    RAM — RAM 3500, 2500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23295·2023-09-28

    Trek Allant+ 7 Bicycles Recalled Due to Brake Hose Crash Hazard

    Trek is recalling about 7,000 Allant+ 7 bicycles with Tektro brakes because the rear brake hose can kink and break when turning the handlebars, causing loss of control and crashes. Trek has received 58 reports of riders losing control, including two minor injuries.

    Product
    Trek Allant+ 7 bicycles with Tektro brakes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23794·2023-09-28

    Secura Air Fryers Recalled Due to Fire and Burn Hazards

    Secura Inc. is recalling approximately 6,400 air fryers because a wire connection can overheat, posing fire and burn hazards. The company has received nine reports of units catching fire, burning, and smoking, though no injuries or property damage have been reported.

    Product
    Secura Air Fryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23296·2023-09-28

    Procter & Gamble Recalls Zevo Fly Insect Spray Over Rupture Hazard

    Procter & Gamble is recalling Zevo Fly, Gnat and Fruit Fly Flying Insect Killer3 Value Packs because the aerosol containers can rupture and leak, posing injury and laceration hazards.

    Product
    Zevo Fly, Gnat and Fruit Fly Flying Insect Killer3 Value Packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23298·2023-09-28

    Rust-Oleum Fluorescent Pink Spray Paint Recalled for Impact Injury Hazard

    Rust-Oleum Professional Fluorescent Pink Inverted Marking Spray Paint cans are recalled because the spray valve assembly can detach with force, creating an impact injury hazard. The company has received five reports of detachment with paint splatter and no injuries reported.

    Product
    Rust-Oleum Professional Fluorescent Pink Inverted Marking Spray Paint cans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2528-2023·2023-09-27

    Intensive Care Ventilators Recalled Due to Capacitor Degradation Risk

    Hamilton Medical is recalling 12 intensive care ventilators (model Hamilton-MR1) due to degrading capacitors that may leak electrolyte, potentially causing ventilation interruption. The recall affects specific serial numbers across the US and Puerto Rico.

    Product
    Hamilton-MR1, REF: 161010, Intensive Care Ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1174-2023·2023-09-27

    Novartis Withdraws SANDIMMUNE Oral Solution Bottles Due to Crystallization

    Novartis is recalling SANDIMMUNE Oral Solution bottles nationwide because they were found to contain crystals. Patients should contact their pharmacy or prescriber about affected bottles.

    Product
    SANDIMMUNE Oral Solution (cyclosporine oral solution, USP) 100 mg/mL, 50 mL bottle, Rx Only, Manufactured by: DELPHARM Huningue S.A.S., Huningue, France, Distributed by: Novartis Pharmaceuticals Corporation, East Hanover, New Jersey 07936, NDC 0078-0110-22.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2529-2023·2023-09-27

    Ventilator Control Board Spare Parts Recalled Due to Electrical Short-Circuit Risk

    Hamilton Medical is recalling 6 control board spare parts for ventilators due to degrading capacitors that may leak electrolyte and cause electrical short circuits, potentially interrupting ventilation.

    Product
    Hamilton C1/T1/MR1, REF: MSP161502/12, Control Board Spare part for ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2530-2023·2023-09-27

    Ventilator Spare Parts Recalled for Degrading Capacitor Risk

    Hamilton Medical is recalling ventilator spare parts (ESM Shielding Set) due to potentially degrading capacitors on the control board. These capacitors may leak electrolyte and cause a short circuit, interrupting ventilation.

    Product
    Hamilton-T1, REF: MSP161339/02, ESM Shielding Set, Spare Part for ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2525-2023·2023-09-27

    Portable Intensive Care Ventilator Recalled for Degrading Capacitor Issue

    Hamilton Medical is recalling 164 Hamilton-C1 portable ventilators due to degrading capacitors that may leak electrolyte, causing electrical short circuits that could interrupt ventilation.

    Product
    Hamilton-C1, REF: 161001, Portable Intensive Care Ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2527-2023·2023-09-27

    Hamilton-T1 Ventilator Recall: Degrading Capacitors May Interrupt Ventilation

    Hamilton Medical recalls 1,216 Hamilton-T1 ventilators due to degrading capacitors on the control board that may leak electrolyte and interrupt ventilation. The recall affects units distributed nationwide in the US and Puerto Rico.

    Product
    Hamilton-T1, REF: 161009, Intensive Care and Transport Ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1517-2023·2023-09-27

    Honey Roasted Sunflower Kernels Recalled for Undeclared Soy and Wheat

    Power Snacks Honey Roasted Sunflower Kernels are being recalled nationwide due to potential undeclared soy and wheat allergens from mislabeling. Approximately 88,084 units are affected.

    Product
    Power Snacks Honey Roasted Sunflower Kernels, Net Wt 1 oz; UPC 076500722025
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2602-2023·2023-09-27

    Stryker ACM System nozzle may disassemble during bone cement mixing

    The break-away femoral nozzle in Stryker's ACM System may disassemble during use, potentially leaving fragments in the surgical site and causing device failure.

    Product
    Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway Nozzle, Restrictors & Prox. Med. Press- Allows the user to mix bone cement with a constant high vacuum through the process. Catalog Number: 0306-705-000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2605-2023·2023-09-27

    Orthopedic hip stem implant recalled due to sterilization failure

    Encore Medical has recalled a hip stem orthopedic implant that was not sterilized before shipment. Non-sterile implants may cause infection if implanted, requiring treatment and potentially revision surgery.

    Product
    DJO Surgical: CLP Hip, Stem, Polished Neck, Lateral Offset Implant, Size#3, REF: 426-11-030
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Food)·F-1534-2023·2023-09-27

    Chocolate Truffles Recalled for Undeclared Yellow Food Dyes

    Fox Confections is recalling F-Bombs Original Truffles due to undeclared Yellow #5 and Yellow #6 food dyes not listed on the label. Consumers with sensitivities to these dyes may be affected.

    Product
    F-Bombs Original Truffles: 12 ounce plastic packaging, plastic packaging is packed into 4x4x2 cardboard boxes. UPC 850036018001
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1540-2023·2023-09-27

    F-Bombs S'Mores Truffles Recalled for Undeclared Yellow Food Dyes

    Fox Confections LLC recalls F-Bombs S'Mores Truffles due to undeclared FD&C Yellow #5 and Yellow #6 food dyes. The product may trigger reactions in individuals sensitive to these colorants.

    Product
    F-Bombs S'Mores Truffles: 12 ounce plastic packaging, plastic packaging is packed into 4x4x2 cardboard boxes. UPC 850036018155
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-2607-2023·2023-09-27

    Orthopedic implant components recalled due to sterilization failure

    Encore Medical is recalling 15 orthopedic implants (DJO Surgical Altivate Reverse) due to sterilization failure. If implanted, unsterilized components may cause infection requiring treatment, monitoring, or revision surgery.

    Product
    DJO Surgical: Altivate Reverse, Humeral Stem, Small Shell, Size 6 x 108mm, REF: 533-06-108
    Category
    Medical Device
    Distribution
    26 states