The Recall Desk

State

Ohio product recalls

72,907 recalls have nationwide distribution and so reach Ohio. 11,719 additional recalls listed Ohio specifically in their distribution scope.

What the numbers show

Total
11,719
Critical
2,106
Severe
2,413
Most recent
2026-09-09

Of the 11,719 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 2,413 (21%) are Severe.

These figures cover only the 11,719 recalls whose distribution notice names Ohio specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1001–1025 of 84626

  • ModerateFDA (Drugs)·D-0698-2026·2026-07-08

    Fungal Fusion antifungal kit recalled for discontinued stability testing

    Blaine Labs Inc is recalling Fungal Fusion ERADICATION Solution kits nationwide because the manufacturer discontinued required stability testing for products still on the market within their expiration dates.

    Product
    Fungal Fusion ERADICATION Solution, Antifungal & Antimicrobial Kit. Contains, 1x2 oz bottle Fungal Fusion Antifungal (Miconazole Nitrate) Cream, 1x2oz bottle Fungal Fusion Antifungal Solution (25% Undecylenic Acid) and 1x1oz bottle of Fungal Fusion Eradication Antimicrobial Show
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2542-2026·2026-07-08

    Medline Convenience Kits recalled for defective Lidocaine Ampules

    Medline Industries is recalling 15,662 Convenience Kits containing Huons Lidocaine HCL Injection USP due to quality issues identified during an FDA manufacturing inspection of the drug supplier's facility.

    Product
    Medline Convenience Kits: 1) SUTURE TRAY, Model Number: SUT12260; 2) CHEST TUBE INSERTION TRAY, Model Number: MNS3390; 3) CONTRACEPTIVE IMPLANT INSERTION KIT, Model Number: MNS9715; 4) 20GX3" RADIAL ART LINE KIT, Model Number: ART351; 5) MYELOGRAM PACK, Model Number: P15
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2660-2026·2026-07-08

    Power-Trialysis Dialysis Catheters Recalled Due to Manufacturing Defects

    Bard Access Systems is recalling Power-Trialysis Short-Term Dialysis Catheters with triple-lumen design due to lidocaine ampoules manufactured under deficient manufacturing practices. The recall affects approximately 8,795 units distributed nationwide and internationally.

    Product
    5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741086953 5605240 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741086977 5605300 Power-Trialysis Short-Term Straight Dialysis C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2543-2026·2026-07-08

    Medline Convenience Kits recalled due to Lidocaine quality issues

    Medline Industries is recalling two convenience kits (Arterial Line Kit and Ultrasound Guided IV Securement Set) due to quality issues with included Lidocaine Ampules identified during an FDA inspection.

    Product
    Medline Convenience Kits: 1) ARTERIAL LINE KIT, Model Number: ART890B; 2) ULTRASOUND GUIDED IV SECUREMENT SET, Model Number: IVS3350
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0654-2026·2026-07-08

    Fexofenadine Hydrochloride Tablets 180 mg Recalled for Impurities

    SUN PHARMACEUTICAL INDUSTRIES INC is recalling Fexofenadine Hydrochloride Tablets, USP 180 mg distributed nationwide because the product failed impurities and degradation specifications. The recall affects approximately 9,048 bottles distributed across the United States.

    Product
    Fexofenadine Hydrochloride Tablets, USP 180 mg, Antihistamine, 150 Tablets per bottle, Distributed by: Ohm Laboratories, Inc., New Brunswick, NJ 08901. NDC 66336-561-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V434000·2026-07-07

    Braun Recalls 2026 Chevrolet Traverse Vehicles Due to Fuel Leak Risk

    Braun is recalling 2026 Chevrolet Traverse vehicles because a missing braze connection on the fuel fill line may allow fuel to leak, increasing the risk of fire.

    Product
    BRAUN — BRAUN CHEVROLET TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V435000·2026-07-07

    Wabash Recalls Econex Refrigerated Bodies Due to Detaching Steps

    Wabash is recalling 2021-2026 Econex Refrigerated Bodies because side door stirrup steps may detach, increasing the risk of injury or a crash.

    Product
    WABASH — WABASH ECONEX REFRIGERATED BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V436000·2026-07-07

    Subaru Ascent, Forester, and Crosstrek vehicles with incorrect weight labels

    Subaru is recalling certain 2019–2026 Ascent, 2025–2026 Forester, and 2026 Crosstrek Hybrid vehicles due to incorrect Gross Axle Weight Rating labels, which may lead to vehicle overload and increased crash risk.

    Product
    SUBARU — SUBARU ASCENT, FORESTER, CROSSTREK HYBRID, FORESTER HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E043000·2026-07-07

    Harbor Freight Recalls Kenway LED Towing and Submersible Light Kits

    Harbor Freight Tools is recalling specific Kenway LED towing and submersible light kits because they may not illuminate properly, increasing crash risk.

    Product
    EXTERIOR LIGHTING:TAIL LIGHTS:BULBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V445000·2026-07-07

    Tesla Recalls 2026 Model Y and 2024 Model 3 for Safety Noncompliance

    Tesla is recalling specific 2026 Model Y and 2024 Model 3 vehicles because they lack required safety features and bumper testing. Owners will be offered a repurchase.

    Product
    TESLA — TESLA MODEL Y, MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E042000·2026-07-06

    Prime-Time Recalls 2025-2026 Ford Med Transit Vans with Wheelchair Retractions

    Prime-Time Specialty Vehicles is recalling 2025-2026 Ford Med Transit vans equipped with Q'Straint Max wheelchair retractors that may fail to lock, posing an injury risk.

    Product
    EQUIPMENT ADAPTIVE/MOBILITY:WHEELCHAIR RESTRAINTS/SECUREMENT:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·26600·2026-07-02

    Junpower CR2032 Lithium Coin Batteries Recalled for Ingestion Hazard

    Junpower CR2032 Batteries (20-piece packs) lack required child-resistant packaging and warning labels. If swallowed, these lithium coin batteries can cause serious internal injuries or death.

    Product
    Junpower CR2032 Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26591·2026-07-02

    VEVOR Baby Loungers Recalled for Entrapment and Fall Hazards

    VEVOR baby loungers sold through multiple retailers from November 2024 through January 2026 are being recalled due to violations of mandatory infant sleep product safety standards. The loungers pose serious risks of fall and entrapment hazards that can cause death or serious injury.

    Product
    VEVOR baby loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V431000·2026-07-02

    Kia Recalls EV6 and EV9 Models Due to Battery Fire Risk

    Kia is recalling 2022-2024 EV6 and 2024 EV9 vehicles because high voltage battery cells may contain misaligned electrodes, creating a fire hazard.

    Product
    KIA — KIA EV9, EV6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26593·2026-07-02

    CVS Health Medicated Hemorrhoidal Wipes Lack Child-Resistant Packaging

    CVS Health Medicated Hemorrhoidal Wipes lack required child-resistant packaging despite containing lidocaine, a substance that poses risk of serious injury or death if ingested by young children.

    Product
    CVS Health Medicated Hemorrhoidal Wipes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V426000·2026-07-02

    Jayco Recalls 2026 Seismic Fifth Wheel Toy Haulers Due to Fire Risk

    Jayco is recalling 2026 Seismic fifth wheel toy haulers because the inverter may lack a grounding connection, increasing the risk of fire and electrical shock.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL SEISMIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26599·2026-07-02

    Metalux Optimized High Bay LED Light Fixtures Recalled for Fire Hazard

    Cooper Lighting recalls about 42,000 Metalux Optimized High Bay LED light fixtures due to a fire hazard. The LED board can overheat or contact combustible materials; nine fires have been reported with no injuries or property damage.

    Product
    Metalux Optimized High Bay (OHB) LED Light Fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26601·2026-07-02

    Metal Wire Bristle Grill Brushes Recalled Over Detachable Bristle Ingestion Hazard

    Conair is recalling about 1.7 million Cuisinart metal wire bristle grill brushes because small wire bristles can detach and be swallowed, posing a risk of serious internal injury. Three consumers have already swallowed bristles and required medical treatment.

    Product
    Metal Wire Bristle Grill Brushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V432000·2026-07-02

    Hyundai Recalls 2023-2024 Ioniq 5 Vehicles Due to Battery Fire Risk

    Hyundai is recalling 2023-2024 Ioniq 5 vehicles because high voltage battery cells may contain misaligned electrodes, posing a fire risk while parked or driving.

    Product
    HYUNDAI — HYUNDAI IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26594·2026-07-02

    POPOOO Jungle Safari LED Finger Lights Recalled for Battery Ingestion Risk

    CPSC has recalled POPOOO Jungle Safari LED Finger Lights sold on Amazon because the toys contain easily accessible button cell batteries that can cause serious injury or death if swallowed. No injuries have been reported.

    Product
    POPOOO Jungle Safari LED Finger Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26E041000·2026-07-02

    Warn Industries Recalls Wireless Remote Kits Due to Winch Movement Risk

    Warn Industries is recalling Wireless Remote Kits (part numbers 90287 and 90289) because the remote control may be incompatible with legacy winches, causing unexpected movement and increasing injury risk.

    Product
    EQUIPMENT:MECHANICAL:WINCH recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide