The Recall Desk

State

Ohio product recalls

73,584 recalls have nationwide distribution and so reach Ohio. 11,764 additional recalls listed Ohio specifically in their distribution scope.

What the numbers show

Total
11,764
Critical
2,112
Severe
2,908
Most recent
2026-10-21

Of the 11,764 recalls naming Ohio we have scored against our rubric, 2,112 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,908 (25%) are Severe.

These figures cover only the 11,764 recalls whose distribution notice names Ohio specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

476–500 of 85348

  • ModerateFDA (Devices)·Z-3222-2026·2026-09-30

    Ventec HomeFill Oxygen System Recalled for Missing Medical Gas Labeling

    Ventec Life Systems is recalling two HomeFill Oxygen Systems because the cylinders lack required medical gas labeling.

    Product
    REF:HF2PC9 HomeFill Oxygen System, HomeFill Cylinder M9 with Integrated Conserver
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3242-2026·2026-09-30

    Philips MR 7700 MRI Systems Recalled for Software Issue

    Philips is recalling 37 MR 7700 MRI systems due to a software issue that can terminate examinations during image reconstruction.

    Product
    MR 7700 and Upgrade to MR 7700; Model Number (REF): 1. 782120, 2. 782153, 3. 782130 (Upgrade);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3233-2026·2026-09-30

    Philips Achieva 3.0T MRI Software Recall for Memory Limit Issues

    Philips is recalling 210 Achieva 3.0T MRI scanners because a software issue can terminate examinations if system memory is exceeded during image reconstruction.

    Product
    Achieva 3.0T; Model Numbers (REF): 1. 781177, 2. 781277, 3. 781278, 4. 781344, 5. 781345;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3262-2026·2026-09-30

    Baxter Recalls PRO+ MRS Mattress Due to UDI Labeling Error

    Baxter Healthcare is recalling 169 PRO+ MRS Mattresses because UDI label errors may lead to incorrect product identification or use with incompatible bed frames.

    Product
    PRO+ MRS SURFACE FOR VERSACARE, mattress with Advanced Microclimate Technology (AMT) uses a non-powered system of intake and output valves to provide weight-based pressure redistribution whenever a patient moves or is repositioned, Model/Catalog Number: P3255A08
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3240-2026·2026-09-30

    Philips Intera 1.5T MRI Systems Recalled for Software Issue

    Philips is recalling 82 Intera 1.5T MRI systems worldwide because a software issue can terminate examinations during image reconstruction if specific scan parameters are manually adjusted.

    Product
    Name (Model Number): 1. Intera 1.5T (781195), 2. Intera 1.5T (781295), 3. Intera 1.5T Achieva IT Nova (781175), 4. Intera 1.5T Achieva Nova (781172), 5. Intera 1.5T Achieva Nova-Dual (781173), 6. Intera 1.5T Omni/Stellar (781104), 7. Intera Achieva 1.5T Pulsar (781171);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3236-2026·2026-09-30

    Philips Ingenia MRI Software Recall for Image Reconstruction Failure

    Philips is recalling 2,038 Ingenia 1.5T MRI systems worldwide due to a software issue that can terminate examinations during image reconstruction if specific scan parameters are manually adjusted.

    Product
    Ingenia 1.5T, Ingenia 1.5T CX and Ingenia 1.5T S; Model Numbers (REF): 1. 781315(1.5T), 2. 781341(1.5T), 3. 781396(1.5T), 4. 782101(1.5T), 5. 782115(1.5T), 6. 782140(1.5T), 7. 781261(1.5T CX), 8. 781262(1.5T CX), 9. 781347(1.5T S);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3263-2026·2026-09-30

    Baxter PRO+ 36-inch Mattress Recalled for UDI Labeling Error

    Baxter Healthcare is recalling 824 PRO+ 36-inch MRS Surface mattresses due to errors in the Unique Device Identification (UDI) label. The discrepancies may lead to incorrect product identification or use with incompatible bed frames.

    Product
    PRO+ 36" MRS SURFACE, mattress with Advanced Microclimate Technology (AMT) uses a non-powered system of intake and output valves to provide weight-based pressure redistribution whenever a patient moves or is repositioned, Model/Catalog Number: P7924A13
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3261-2026·2026-09-30

    AVID Medical Recalls Halyard IV Start Kits Due to Packaging Seal Issues

    AVID Medical is recalling 192 Halyard IV Start Kits because the included BD ChloraPrep applicators may have open or incomplete packaging seals.

    Product
    Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3243-2026·2026-09-30

    Philips MRI Software Recall for Image Reconstruction Failure

    Philips is recalling SmartPath MRI software due to a defect that can terminate examinations during image reconstruction if system memory is exceeded.

    Product
    SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T, SmartPath to dStream for XR and 3.0T, SmartPath to Ingenia Elition X; Model Numbers (REF): 1. 781260 (1.5T), 2. 782112 (1.5T), 3. 782146 (1.5T), 4. 782145 (3.0T), 5. 781270 (XR and 3.0T), 6. 782113 (XR and 3.0T), 7.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3234-2026·2026-09-30

    Philips Achieva XR MRI Systems Recalled for Software Memory Issue

    Philips is recalling 15 Achieva XR MRI systems because a software issue can terminate examinations if scan parameters exceed system memory.

    Product
    Achieva XR; Model Numbers (REF): 1. 781153, 2. 781253;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3239-2026·2026-09-30

    Philips Ingenia MRI Software Recall for Image Reconstruction Failure

    Philips is recalling 596 Ingenia Elition MRI systems due to a software issue that can terminate examinations during image reconstruction if system memory is exceeded.

    Product
    Ingenia Elition S and Ingenia Elition X; Model Numbers (REF): 1. 781357(S), 2. 782106(S), 3. 782137(S), 4. 781358(X), 5. 782107(X), 6. 782119(X), 7. 782136(X), 8. 782158(X);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1394-2026·2026-09-30

    So Delicious Dairy Free Salted Caramel Cluster Cashewmilk Recalled for Foreign Material

    WWF Operating Company is recalling So Delicious Dairy Free Salted Caramel Cluster Cashewmilk because it may contain small stones and other hard objects.

    Product
    So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert. 16 oz paper tub with an attached paper lid. Sold as a single unit multi serving tub. UPC 744473 476138. Distributed by For So Delicious Dairy Free Eugene, OR 97402.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3260-2026·2026-09-30

    AVID Medical Recalls Halyard IV Start Kits Due to Packaging Seal Issues

    AVID Medical is recalling Halyard IV Start Kits because the included BD ChloraPrep applicators may have open or incomplete packaging seals.

    Product
    Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3221-2026·2026-09-30

    Ventec HomeFill Oxygen Cylinder Recall for Missing Medical Gas Labeling

    Ventec Life Systems is recalling 21 HomeFill Oxygen System cylinders because they lack required medical gas labeling.

    Product
    HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0867-2026·2026-09-30

    Macleods Recalls Olanzapine Tablets Due to Impurity Levels

    Macleods Pharmaceuticals is recalling Olanzapine 5 mg tablets because organic and unspecified impurities exceeded specifications.

    Product
    OLANZAPINE — OLANZAPINE (OLANZAPINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V622000·2026-09-29

    Chrysler Recalls 2026 Ram 1500 Vehicles for Side Air Bag Defect

    Chrysler is recalling 2026 Ram 1500 vehicles because side air bag connectors may not be secured properly, potentially preventing deployment in a crash.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V623000·2026-09-29

    RAM Recalls 2026 Ram 1500 Vehicles for Tire Pressure Sensor Defect

    Chrysler is recalling 2026 Ram 1500 vehicles because tire pressure sensors may fail to detect low pressure or illuminate the warning light, increasing crash risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V621000·2026-09-29

    Ram Promaster Recall Issued for Electric Power Steering Wiring Defect

    Chrysler is recalling 2022-2026 Ram Promaster and 2024-2026 Ram 3500 Electric vehicles because water may enter the steering wiring harness, potentially disabling power steering assist.

    Product
    RAM — RAM PROMASTER, PROMASTER BEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V619000·2026-09-28

    Volvo Recalls VNL and VNR Trucks for Braking Software Defect

    Volvo Trucks North America is recalling 2025-2027 VNL and 2026-2027 VNR trucks with tanker packages due to inaccurate axle load calculations that may reduce braking performance.

    Product
    VOLVO — VOLVO VNL (4), VNR (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E066000·2026-09-28

    Cummins Recalls L9 Diesel Engines Due to Fuel Hose Separation Risk

    Cummins is recalling L9 diesel engines because remote fuel filter hoses may separate, causing fuel leaks, engine stalls, and increased fire or crash risks.

    Product
    FUEL SYSTEM, DIESEL:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V618000·2026-09-25

    ATC Recalls RM900 and RM700 Trailers Due to Coupler Bolt Loosening

    ATC is recalling 2024-2026 RM900 and 2026 RM700 trailers because coupler mounting bolts may loosen, potentially separating the coupler and increasing crash risk.

    Product
    ATC — ATC RM900, RM700
    Category
    Vehicle
    Distribution
    Distributed nationwide