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.

601–625 of 84538

  • ModerateFDA (Drugs)·D-0735-2026·2026-07-29

    Dabigatran Etexilate Capsules Recalled Over Impurity Test Failure

    Ascend Laboratories is recalling 1,753 cartons of dabigatran etexilate capsules (lot 25141707) due to out-of-specification results in impurity testing during 12-month stability studies.

    Product
    DABIGATRAN ETEXILATE — DABIGATRAN ETEXILATE (DABIGATRAN ETEXILATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0725-2026·2026-07-29

    Glycopyrrolate Injection Recall Due to Hair Contamination

    Fresenius Kabi is recalling Glycopyrrolate Injection due to the presence of particulate matter, specifically hair found in the product.

    Product
    GLYCOPYRROLATE — GLYCOPYRROLATE (GLYCOPYRROLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2763-2026·2026-07-29

    Halyard EYE PACK Convenience Kits Recalled Due to Incorrect Betadine Concentration

    AVID Medical, Inc. is recalling certain Halyard EYE PACK convenience kits because the Betadine solution contained within them has an incorrect concentration.

    Product
    Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0712-2026·2026-07-29

    FDA Recalls Amlodipine and Olmesartan Tablets Over Failed Dissolution Test

    Ascend Laboratories is recalling 6,192 bottles of Amlodipine and Olmesartan Medoxomil tablets nationwide due to failed dissolution specifications and Olmesartan content below specifications.

    Product
    AMLODIPINE AND OLMESARTAN MEDOXOMIL — AMLODIPINE AND OLMESARTAN MEDOXOMIL (AMLODIPINE AND OLMESARTAN MEDOXOMIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0729-2026·2026-07-29

    FDA Recalls Xylocaine Injections Due to Hair Contamination

    FDA is recalling Xylocaine (lidocaine HCl) injections due to the presence of particulate matter, specifically hair found in the product.

    Product
    XYLOCAINE — XYLOCAINE (LIDOCAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2761-2026·2026-07-29

    Olympus 4K UHD LCD Monitors Recalled Due to Potential Connector Faults

    Olympus Corporation of the Americas is recalling 10 Olympus 4K UHD LCD Monitors (Model OEV321UH) because the HDMI and DisplayPort connectors may become faulty.

    Product
    Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual display unit designed for displaying graphical information in color.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2790-2026·2026-07-29

    Medline Medical Convenience Kits Recalled Due to Potential Bacillus Contamination

    Medline Industries, LP is recalling specific Medline NEURO PACK convenience kits because they may contain low levels of Bacillus species contamination.

    Product
    Medline medical convenience kits labeled as: NEURO PACK, Medline Kit SKU DYNJ59397P
    Category
    Medical Device
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-2773-2026·2026-07-29

    Pipeline Flex Embolization Devices Recalled Due to Incorrect Labeling of Implant Length

    Micro Therapeutics, Inc. is recalling Pipeline Flex Embolization Devices because the labeled implant length does not match the actual device length.

    Product
    Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 12 mm 027 REF PED2-300-12. Intracranial aneurysm flow diverter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2774-2026·2026-07-29

    Embolization devices recalled due to incorrect labeling of implant dimensions

    Micro Therapeutics, Inc. is recalling Pipeline Flex Embolization Devices because the labels may incorrectly state the implant length.

    Product
    Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 20 mm 027 REF PED2-300-20. Intracranial aneurysm flow diverter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2769-2026·2026-07-29

    Silent Nite Sleep Appliance Recalled Due to Lack of FDA Clearance

    Prismatik Dentalcraft, Inc. is recalling Silent Nite Sleep Appliances because the device does not have FDA clearance.

    Product
    Brand Name: Silent Nite Product Name: Silent Nite Sleep Appliance Model/Catalog Number: SILNT Product Description: Silent Nite Sleep Appliance is a mandibular advancement device (MAD) intended to treat snoring and mild to moderate obstructive sleep apnea (OSA).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0758-2026·2026-07-29

    Supernus Recalls Trokendi XR Capsules for Failed Dissolution Specifications

    Supernus Pharmaceuticals is recalling Trokendi XR (topiramate) capsules because they failed dissolution specifications. The recall covers 15,853 bottles distributed nationwide.

    Product
    TROKENDI XR — TROKENDI XR (TOPIRAMATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V488000·2026-07-28

    Newell Recalls 2025-2027 P50 Coaches Due to Air Spring Defect

    Newell Coach Corp. is recalling 2025-2027 P50 coaches because the steer axle air spring base may crack, potentially causing loss of suspension support and increasing crash risk.

    Product
    NEWELL — NEWELL P50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V487000·2026-07-28

    Ford Recalls 2023-2025 Mustang Mach E for Rear Window Trim Defect

    Ford is recalling 2023-2025 Mustang Mach E vehicles because rear side quarter window glass trim may detach, creating a road hazard and increasing crash risk.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V484000·2026-07-27

    Jayco Recalls 2024-2026 Entegra Motorhomes Due to Brake Light Defect

    Jayco is recalling certain 2024-2026 Entegra motorhomes because exterior brake lights may stay on when brakes are not applied, increasing crash risk.

    Product
    ENTEGRA — ENTEGRA REATTA XL, CORNERSTONE RESERVE, REATTA, ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V486000·2026-07-27

    Foretravel Recalls Realm Motorcoaches Due to Brake Light Defect

    Foretravel is recalling 2025-2027 Realm and Realm Presidential motorcoaches because exterior brake lights may stay on, increasing crash risk.

    Product
    FORETRAVEL — FORETRAVEL REALM PRESIDENTIAL, REALM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V483000·2026-07-27

    Jayco Recalls 2026 Entegra Anthem Motorhomes for Incorrect Tire Label

    Jayco is recalling 2026 Entegra Anthem motorhomes because the vehicle certification label may list the wrong tire size, which could lead to installing incorrect replacement tires.

    Product
    ENTEGRA — ENTEGRA ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V481000·2026-07-24

    Mercedes-Benz Recalls Various Models Due to Driver's Door Lock Defect

    Mercedes-Benz USA, LLC is recalling certain 2020-2026 Mercedes-Benz vehicles because a faulty door lock micro-switch may cause the vehicle to roll away.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLA 35, AMG GLB35 4MATIC, AMG GLC43 4MATIC, GLC 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V480000·2026-07-24

    Yamaha Boat Trailer Recall Issued Due to Tongue Failure Risk

    Midwest Industries is recalling 2027 Yamaha boat trailers because the tongue may fail during towing, causing the trailer to detach and increasing crash risk.

    Product
    YAMAHA — YAMAHA BOAT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide