The Recall Desk

State

Ohio product recalls

73,366 recalls have nationwide distribution and so reach Ohio. 11,756 additional recalls listed Ohio specifically in their distribution scope.

What the numbers show

Total
11,756
Critical
2,117
Severe
2,903
Most recent
2026-10-07

Of the 11,756 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 2,903 (25%) are Severe.

These figures cover only the 11,756 recalls whose distribution notice names Ohio specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18151–18175 of 85122

  • SevereFDA (Food)·F-0829-2023·2023-05-17

    Revolution Farms Salad Kit Recalled for Listeria Contamination

    Revolution Farms Zesty Southwest salad kits are being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed in Michigan, Ohio, and Wisconsin.

    Product
    Revolution Farms Zesty Southwest 6oz salad kit in plastic container UPC 856791008240
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0841-2023·2023-05-17

    Vitamin B Capsules Recalled for Undeclared Milk Allergen

    EuroMedica and Terry Naturally vitamin B complex capsules are being recalled nationwide due to undeclared milk allergen. Consumers with milk allergies should not use these products.

    Product
    Multiple Vitamin B Capsules, 60 Capsules, Biologically Active Forms of Vitamin B12, Folate, B6. Packaged in bottles under the following brands: 1. EuroMedica Active B Complex, Product #68006, UPC 3 67703 68006 0. Manufactured by a cGMP compliant facility exclusively for…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0834-2023·2023-05-17

    Meijer Tomato Caprese Salad Recalled Due to Listeria Risk

    Meijer is recalling Fresh From Meijer Tomato Caprese Salad due to potential Listeria monocytogenes contamination. The product was distributed to stores across six states.

    Product
    Fresh From Meijer Tomato Caprese Salad 6 Oz UPC - 713733246101
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0835-2023·2023-05-17

    Meijer Mediterranean Salad Recalled Due to Listeria Contamination

    Meijer Inc is recalling Fresh From Meijer Mediterranean Salad due to potential Listeria monocytogenes contamination. Approximately 1,064 units were distributed to Meijer stores in six Midwest states.

    Product
    Fresh From Meijer Mediterranean Salad - 6.5 Oz UPC - 713733246132
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0567-2023·2023-05-17

    Atovaquone Oral Suspension Recalled for Bacillus cereus Contamination

    Camber Pharmaceuticals is recalling Atovaquone Oral Suspension due to contamination by Bacillus cereus bacteria. The contamination was discovered during testing of repackaged medication.

    Product
    ATOVAQUONE — ATOVAQUONE (ATOVAQUONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0840-2023·2023-05-17

    Salad Product Recalled by Meijer for Listeria Contamination

    Meijer Inc is recalling Fresh From Meijer Cranberry Spinach Shareable Salad due to potential Listeria monocytogenes contamination. The product was distributed to Meijer stores in Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin.

    Product
    Fresh From Meijer Cranberry Spinach Shareable Salad 12 Oz UPC - 708820304321
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1428-2023·2023-05-17

    Cook Blue Rhino G2 Tracheostomy Introducer Trays Recalled for Connection Defect

    Cook Incorporated is recalling Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Trays because the device connectors are not making secure connections with 15mm caps and other circuit components, resulting in unsecure connections.

    Product
    Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray, Reference Part Numbers C-PTISYJ-100-HC-G-EU-FLEX8.5 (G57725), C-PTISYJ-100-HC-G-NA-FLEX7.5 (G57720), C-PTISYJ-100-HC-G-NA-FLEX8.5 (G57721), C-PTISY-100-HC-G-NA-FLEX8.5 (G57717), C-PTISY-100-HC-G-NA-FLEX7.5 (G57716)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0831-2023·2023-05-17

    Meijer Chicken Caesar Salads Recalled Due to Listeria monocytogenes Contamination

    Meijer Inc. is recalling Fresh From Meijer Chicken Caesar Salads (6.4 oz and 10 oz sizes) due to potential Listeria monocytogenes contamination. Products were distributed to Meijer stores in six states: Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin.

    Product
    Fresh From Meijer Chicken Caesar Salad 6.4 Oz UPC - 760236117452 Fresh From Meijer Chicken Caesar Shareable Salad 10 Oz UPC - 719283679338
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·23V349000·2023-05-17

    Foretravel Recalls 2022-2024 Motorhomes Due to Software Error

    Foretravel is recalling 2022-2024 Realm, FS450, and Realm Presidential motorhomes because a software error may cause loss of drive power or disable safety systems.

    Product
    FORETRAVEL — FORETRAVEL REALM, FS450, REALM PRESIDENTIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0828-2023·2023-05-17

    Revolution Farms Salad Kits Recalled for Listeria Contamination

    Revolution Farms is recalling Traverse City Cherry 6-ounce salad kits due to potential Listeria monocytogenes contamination. Affected products were distributed in Michigan, Ohio, and Wisconsin.

    Product
    Revolution Farms Traverse City Cherry 6oz salad kit in plastic container UPC 856791008226
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0827-2023·2023-05-17

    Revolution Farms Sesame Ginger Crunch Salad Kit Recalled for Listeria Monocytogenes

    Revolution Farms Sesame Ginger Crunch 6oz salad kits (UPC 856791008233, 'Sell By 3/23/23') are recalled due to potential Listeria monocytogenes contamination. Affected units were distributed in Michigan, Ohio, and Wisconsin.

    Product
    Revolution Farms Sesame Ginger Crunch 6oz salad kit in plastic container UPC 856791008233
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0832-2023·2023-05-17

    Meijer Chicken Cobb Salad Recalled Due to Listeria Contamination Risk

    Meijer Inc. is recalling Fresh From Meijer Chicken Cobb Salad due to potential Listeria monocytogenes contamination. The product was distributed to Meijer stores in six states.

    Product
    Fresh From Meijer Chicken Cobb Salad 8.8 Oz UPC - 719283679321
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0824-2023·2023-05-17

    Revolution Farms Romaine Lettuce Recalled for Listeria Contamination

    Revolution Farms romaine lettuce products distributed in Michigan, Ohio, and Wisconsin are recalled due to potential Listeria monocytogenes contamination. Consumers should not consume affected products and should discard them.

    Product
    Revolution Farms Robust Romaine plastic 5oz Retail container UPC 856791008035 and 3lb bulk clear poly bag UPC 856791008127 Revolution Farms Romaine Lettuce Boats plastic 5oz Retail container UPC 856791008196 Revolution Farms Whole Leaf Romaine plastic 5oz Retail container UPC…
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1564-2023·2023-05-17

    Bard Mission Biopsy Instrument Kit cannula and needle incompatibility

    Bard Mission Disposable Biopsy Instrument Kit has an incompatibility defect where the cannula is oversized relative to the needle, preventing proper insertion and tissue access. This could cause procedure delays and insufficient tissue collection.

    Product
    Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK, 20G x 16CM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1577-2023·2023-05-17

    STA Compact Max analyzer firmware bug causes inaccurate test results

    A firmware bug in Diagnostica Stago's STA Compact Max analyzer causes intermittent shortened coagulation times and frequent technical errors that produce inaccurate lab test results. Five units were distributed to clinical laboratories nationwide.

    Product
    STA Compact Max fully automatic clinical analyzer, Reference Numbers 58602 and 58612
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0830-2023·2023-05-17

    Ziyad Cinnamon Powder Recalled for Elevated Lead Levels

    ZB Importing LLC is recalling Ziyad cinnamon powder (4.5 oz jars) from lot 21321G2 due to elevated lead levels. The recall affects 3,456 units distributed across multiple U.S. states and territories.

    Product
    Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432, 12 retail jars per wholesale case
    Category
    Food
    Distribution
    35 states
  • HighFDA (Devices)·Z-1575-2023·2023-05-17

    STA R Max Analyzer Firmware Bug Produces Inaccurate Coagulation Test Results

    Diagnostica Stago is recalling the STA R Max fully automatic clinical analyzer due to a firmware bug that causes intermittent shortened coagulation times and increased technical errors, potentially producing inaccurate blood clotting test results.

    Product
    STA R Max fully automatic clinical instrument designed to perform tests on human plasmas, Reference Numbers 59013 and 59026
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1572-2023·2023-05-17

    APLS IgM Diagnostic Reagent Packs Recalled Due to Incorrect Conjugate

    Bio-Rad Laboratories is recalling 932 BioPlex 2200 APLS IgM Reagent Packs (Lot 301538) nationwide because they were packaged with incorrect conjugate. This could result in false-positive and false-negative test results.

    Product
    BioPlex 2200 REF 665-2050, APLS IgM Pack, APLS IgM Reagent Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1579-2023·2023-05-17

    BD Pyxis MedStation ES software failure causes patient data loss

    BD Pyxis automated dispensing cabinet software versions 1.7.0 through 1.7.4 experience download failures causing partial loss of patient information and transaction data. This may result in dispensing incorrect medication doses, allergenic medications, or discontinued medications.

    Product
    BD Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation ES (Med ES Main Tower), REF: 352; BD Pyxis Anesthesia Station ES, REF: 327; BD Pyxis CII Safe ES Tower Main, REF: 1116-00; BD Pyxis CII Safe ES, Desktop PC, W-LESS SCNR, BIO, REF: 107-255-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1576-2023·2023-05-17

    STA Compact Analyzer Firmware Bug Causes Inaccurate Test Results

    Diagnostica Stago is recalling STA Compact Analyzers due to a firmware bug causing intermittent shortened coagulation times and increased technical errors. No illnesses or injuries have been reported.

    Product
    STA Compact Automated Multi-Parametric Analyzer, Reference Numbers 58602 and 58612
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1569-2023·2023-05-17

    Aesculap Caiman Articulating Surgical Device Recalled for Loose Spring

    Aesculap Caiman Articulating electrosurgical devices are being recalled because a spring may become loose and fall out during surgery, potentially entering the patient's body.

    Product
    Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and coagulation device for cutting/coagulation/ablation during endoscopic (including laparoscopic, arthroscopic) surgery, and may in addition be intended for open surgery. Product Code: PL771SU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1573-2023·2023-05-17

    Laboratory Management Software May Display Incorrect Slide Labels

    TDHisto/Cyto laboratory management software may display incorrect information on slide labels in specific use cases. The FDA has issued a Class II recall affecting laboratories nationwide in California.

    Product
    TDHisto/Cyto - A software product used for managing medical information in the field of laboratories performing histology, nongynecological and gynecological cytology and autopsy activities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1570-2023·2023-05-17

    M-Close Kit suturing apparatus recalled due to plastic housing fracture risk

    New Wave Endo-Surgical is recalling the M-Close Kit surgical suturing apparatus because the plastic housing may fracture. The recall affects 295 units distributed in Florida, Massachusetts, and Georgia.

    Product
    M-Close Kit, REF 27-101; a disposable, ligature passing, suturing apparatus and needle guide for the abdominal wall
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0570-2023·2023-05-17

    Gabapentin tablets recalled due to product mixup with foreign tablet

    The Harvard Drug Group recalled 3,984 cartons of Gabapentin 600 mg tablets distributed nationwide due to a product mixup where one foreign tablet was found.

    Product
    GABAPENTIN — GABAPENTIN (GABAPENTIN)
    Category
    Drug
    Distribution
    Distributed nationwide