The Recall Desk

State

Ohio product recalls

72,820 recalls have nationwide distribution and so reach Ohio. 11,718 additional recalls listed Ohio specifically in their distribution scope.

What the numbers show

Total
11,718
Critical
2,106
Severe
2,412
Most recent
2026-09-02

Of the 11,718 recalls naming Ohio we have scored against our rubric, 2,106 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,412 (21%) are Severe.

These figures cover only the 11,718 recalls whose distribution notice names Ohio specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

701–725 of 84538

  • ModerateFDA (Devices)·Z-2732-2026·2026-07-22

    Orthofix MINIRAIL External Fixation Devices Incorrectly Labeled

    Orthofix MINIRAIL unilateral external fixation devices may be labeled with incorrect model numbers. Three model variants (M101, M103, M122) were mislabeled during manufacturing.

    Product
    Orthofix MINIRAIL, ARTICULATED, FIXATOR, VERTICAL AXIS REF: M122, Unilateral orthopedic/trauma external fixation device
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-2744-2026·2026-07-22

    Photera 600 3-D phototherapy device UV sensor calibration error recall

    Daavlin Distributing Company is recalling Photera 600 3-D phototherapy devices because the UV sensor gain calculation is incorrect, causing inaccurate ultraviolet output measurement.

    Product
    Photera 600 3-D, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0684-2026·2026-07-22

    Good Neighbor Pharmacy Earwax Removal Drug Recalled for Low Potency

    Bell Pharmaceuticals is recalling Good Neighbor Pharmacy Earwax Removal (Carbamide Peroxide 6.5%) due to subpotency—the active ingredient concentration is significantly reduced from expected levels, and the product has a low pH.

    Product
    GOOD NEIGHBOR PHARMACY EARWAX REMOVAL — GOOD NEIGHBOR PHARMACY EARWAX REMOVAL (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2722-2026·2026-07-22

    da Vinci SP Instrument Arm Drape may detach during surgical procedures

    Intuitive Surgical is recalling da Vinci SP Instrument Arm Drapes because the drape rings may detach, exposing the instrument arm and potentially delaying procedures. The recall affects 11,113 units distributed worldwide.

    Product
    da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0679-2026·2026-07-22

    Clinere Ear Wax Remover Recalled for Subpotent Carbamide Peroxide

    Bell Pharmaceuticals is recalling Clinere Ear Wax Remover nationwide because the product contains significantly reduced active ingredient and low pH. The affected lots were distributed throughout the United States.

    Product
    CLINERE EAR WAX REMOVER — CLINERE EAR WAX REMOVER (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2743-2026·2026-07-22

    Photera 600 Phototherapy Device UV Sensor Calibration Error

    Daavlin Distributing Company is recalling 26 Photera 600 phototherapy devices nationwide because the UV sensor gain calibration is incorrect, causing inaccurate ultraviolet output readings.

    Product
    Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2736-2026·2026-07-22

    Medline Kits with Zimmer Biomet Mixing Bowls Recalled for Seal Defects

    Medline is recalling 163 kits containing Zimmer Biomet mixing bowls and spatulas due to seal nonconformities that may compromise sterility. The defect could require extended surgery time to locate an alternative device.

    Product
    Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0688-2026·2026-07-22

    CAREone Earwax Removal Drops Recalled for Subpotent Active Ingredient

    CAREone Earwax Removal Drops (Carbamide Peroxide 6.5%) are recalled because the product contains significantly reduced active ingredient (~0.6% vs. expected ~6–7%) and low pH, making it ineffective.

    Product
    CAREONE EARWAX REMOVAL DROPS — CAREONE EARWAX REMOVAL DROPS (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0683-2026·2026-07-22

    Family Wellness Carbamide Peroxide Earwax Removal Kit Subpotent Drug

    Family Wellness Carbamide Peroxide 6.5% earwax removal kits are being recalled because they are subpotent with low pH and significantly reduced active ingredient content (approximately 0.6% versus the expected 6–7%). Consumers should stop using affected lots and consult their pharmacist.

    Product
    FAMILY WELLNESS EARWAX REMOVAL EARWAX AND BULB — FAMILY WELLNESS EARWAX REMOVAL EARWAX AND BULB (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2740-2026·2026-07-22

    Rio II Nasal Pillows Interface Packaging and Labeling Discrepancy Recall

    3B Medical, Inc. is recalling Rio II Nasal Pillows Interface devices due to packaging and labeling discrepancies involving product size identification and device identifiers. The affected models are RII1001 (Small), RII1002 (Medium), and RII1003 (Large).

    Product
    Brand Name: Rio" II Product Name: Rio" II Nasal Pillows Interface Model/Catalog Number: RII1001 (Small), RII1002 (Medium), RII1003 (Large) Software Version: N/A Product Description: Nasal pillows interface intended for use with positive airway pressure therapy devices. The de
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V470000·2026-07-21

    Ford Recalls 2025-2027 Explorer and Lincoln Aviator for Seat Recline Issue

    Ford is recalling 76,748 2025-2027 Explorer and Lincoln Aviator vehicles because an unoccupied driver's seat may recline unintentionally, potentially trapping a second-row occupant.

    Product
    FORD — FORD, LINCOLN EXPLORER, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowNHTSA·26V469000·2026-07-21

    Ember Recalls 2027 Travel Trailers Due to Incorrect VIN Labels

    Ember is recalling 2027 E-Series, Touring, and Overland travel trailers because the Federal Certification Label may list the wrong VIN, which could prevent owners from recognizing safety recalls.

    Product
    EMBER — EMBER E-SERIES, TOURING EDITION, OVERLAND SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V467000·2026-07-20

    Blue Bird Recalls 2022-2027 Vision Transit Buses for Brake Line Damage

    Blue Bird is recalling 2022-2027 Vision transit buses because an exhaust hanger pin may damage the hydraulic brake line, causing leaks and increasing fire or crash risks.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V466000·2026-07-20

    Blue Bird Vision School Buses Recalled Due to Brake Line Fire and Crash Risk

    Blue Bird is recalling certain 2022-2027 Vision school buses because an exhaust hanger cotter pin may damage hydraulic brake lines, causing leaks that increase the risk of fire or crashes.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V463000·2026-07-17

    Altec Recalls 2024-2026 AT Series Vehicles Due to Bearing Fastener Defect

    Altec is recalling 2024-2026 AT Series vehicles because turntable rotation bearing fasteners may not have been heat treated properly, posing a risk of component separation and injury.

    Product
    ALTEC — ALTEC AT SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V462000·2026-07-17

    Turtle Top Recalls 2026 Terra Ford Transit Buses Due to Lift Control Failure

    Turtle Top is recalling 2026 Terra Ford Transit buses because an electrical contactor may fail, preventing the wheelchair lift from stopping. This defect increases the risk of injury.

    Product
    TURTLE TOP — TURTLE TOP TERRA FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V465000·2026-07-17

    Great Dane Recalls 2027 Champion Trailers for Rear Impact Guard Defect

    Great Dane is recalling 2027 Champion dry van trailers because they may lack required rear impact guard extension channels, increasing injury risk in crashes.

    Product
    GREAT DANE — GREAT DANE CHAMPION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V464000·2026-07-17

    Foretravel Recalls 2027 Realm Motorcoaches Due to Fire Risk

    Foretravel is recalling 2027 Realm Presidential Motorcoaches because a fan assembly circuit board may overheat, increasing the risk of a fire.

    Product
    FORETRAVEL — FORETRAVEL REALM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26C004000·2026-07-17

    Evenflo Recalls Reo by Revolve360 Child Seats for Headrest Shift Risk

    Evenflo is recalling specific Reo by Revolve360 child seats because the headrest may shift during a crash, increasing injury risk.

    Product
    CHILD SEAT:SHELL:HEADREST:LOCKING MECHANISM recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V460000·2026-07-16

    IC Bus EVSB and CESB school buses recalled for structural body joint defects

    International Motors, LLC is recalling certain 2025-2027 IC Bus EVSB and CESB school buses due to insufficient epoxy coverage on body joints. This defect may cause panels to separate during a crash.

    Product
    IC BUS — IC BUS CESB, EVSB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V459000·2026-07-16

    2023–2027 International MV and HV vehicles battery cable fire risk

    International Motors is recalling certain 2021, 2023–2027 MV and 2026–2027 HV vehicles. The battery interconnect cable may contact adjacent components, creating a short circuit that increases fire risk.

    Product
    INTERNATIONAL — INTERNATIONAL HV, MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26627·2026-07-16

    Noerishia Adult Portable Bed Rails Recalled for Entrapment and Asphyxiation Risk

    Noerishia Adult Portable Bed Rails sold on Amazon violate the mandatory safety standard and pose a risk of serious injury or death from entrapment and asphyxiation. Users can become entrapped within the rail or between the rail and mattress.

    Product
    Noerishia Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26622·2026-07-16

    Wade Logan Annyka 9-Drawer Fabric Dressers Recalled for Tip-Over Risk

    About 180 Wade Logan Annyka 9-Drawer Fabric Dressers sold online at Wayfair.com from September 2023 through May 2026 are being recalled because they can tip over and pose entrapment hazards to children if not anchored to the wall.

    Product
    Wade Logan Annyka 9-Drawer Fabric Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide