The Recall Desk

State

Ohio product recalls

20,364 recalls have nationwide distribution and so reach Ohio. 0 additional recalls listed Ohio specifically in their distribution scope.

About recalls in Ohio

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Ohio consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

15726–15750 of 20364

  • SevereFDA (Food)·F-1657-2022·2022-09-07

    Sated Complete Keto Meal Shake Chocolate recalled for potential bacterial contamination

    Lyons Magnus, Inc. recalls Sated Complete Keto Meal Shake Chocolate Flavor due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. More than 53 million units distributed nationwide.

    Product
    Sated Complete Keto Meal Shake Chocolate Flavor. 11 fl oz (325ml) UPC 8 57227-00721 9. 12 Count Case UPC 00857227007219. Distributed by LongRun LLC, Belmont, MA 02478. Important: Must be refrigerated after opening to maintain safety.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1604-2022·2022-09-07

    Aloha Organic Protein Drink recalled for Cronobacter and botulism contamination

    Lyons Magnus recalls Aloha Organic Protein Drink nationwide due to Cronobacter sakazakii and Clostridium botulinum contamination. The FDA Class I recall affects 53,818,025 units.

    Product
    Aloha Organic Protein Drink, Coconut Plant-based protein. Net 11 FL OZ (330 mL) Tetra Pak container UPC 8 42096-11237 9. Sold in 4 count package wrap with UPC 842096122378. Shake Well. Best Chilled. Manufactured for: Aloha, Littleton, CO 80127
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1643-2022·2022-09-07

    Stumptown Cold Brew Coffee Recalled Nationwide for Bacterial Contamination

    Lyons Magnus Inc. is recalling Stumptown Cold Brew Coffee with Cream & Sugar nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum bacteria.

    Product
    Stumptown Cold Brew Coffee with Cream & Sugar Chocolate. 11 Fl Oz. 325 ML. UPC 8 55186-00686 1. Sold in 12-count case UPC 108551860006861. Manufactured for Stumptown Coffee Roasters, 100 SE Salmon St. Portland, OR 97214
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1632-2022·2022-09-07

    Sysco Imperial Med Plus Vanilla Nutritional Drink Recalled for Bacterial Contamination

    Lyons Magnus recalls Sysco Imperial Med Plus Vanilla Nutritional Drink nationwide for Cronobacter sakazakii and Clostridium botulinum contamination. The recall affects 53,818,025 units.

    Product
    Sysco Imperial Med Plus 2.0 Vanilla Nutritional Drink. High Calorie, High Protein. Mildly Thick Nectar Consistency. 32 FL OZ (1 QT) 946mL UPC 0 74865-92730 7. Reorder # 0108910. 12 count case UPC 10074865927304. Refrigerate prior to serving. Shake well. Refrigerat
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1607-2022·2022-09-07

    Cold Coffee Recalled Nationwide for Bacterial Contamination Risk

    Intelligentsia Cold Coffee in 10.9 oz containers is recalled nationwide due to potential Cronobacter sakazakii and Clostridium botulinum contamination. Consumers should not consume the product.

    Product
    Intelligentsia, Cold Coffee. Net 10.9 fl oz (325 mL) Tetra Pak container UPC 8 00222-00096 9. Shake Best enjoyed cold. Refrigerate after opening. Produced for: Intelligentsia Coffee, Inc., Aloha, Chicago, IL 60612.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1600-2022·2022-09-07

    Abbott Glucerna Rich Chocolate Shake recalled nationwide for pathogenic bacteria

    Lyons Magnus is recalling Glucerna original Rich Chocolate Shake nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The recall affects approximately 53.8 million units distributed across the U.S.

    Product
    Glucerna original Rich Chocolate Shake, 8 FL OZ (237 mL). Delicious Snack or Small Meal Replacement. UPC 0 70074-68565 6. Sold in 24 count case, UPC Case 0070074685649. Shake Well. Serve cold. Refrigerate after opening. Manufactured for: Abbott Nutrition, Abbott Labora
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1667-2022·2022-09-07

    Kate Farms Nutrition Shake recalled for potential bacterial contamination

    Kate Farms Nutrition Shake (Coffee, 11 fl oz) is being recalled nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The recall affects products with lot codes 7331 and 8031.

    Product
    kate farms Nutrition Shake, Coffee. 11 fl oz (325 mL) UPC 8 11112-03062 1. 12 count case UPC 00811112030638. Shake Well. After opening, refrigerate and use within 4 days. Made for Kate Farms, Inc., 101 Innovation Place, Santa Barbara, CA 93708
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1660-2022·2022-09-07

    Lyons Barista Frappe Base recalled for bacterial contamination

    Lyons Magnus is recalling Barista Style Sweet Cream Frappe Base nationwide due to findings of and potential for Cronobacter sakazakii and Clostridium botulinum.

    Product
    Lyons Barista Style Sweet Cream Frappe Base 32 fl oz (1qt) 946 mL. UPC 0 45796-10089 3. Shake well before using. After opening, keep refrigerated and use within 7 days. 4count Case UPC 629046564019.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1519-2022·2022-09-07

    Medtronic endotracheal tubes recalled for reported airway obstruction risk

    Medtronic Xomed is recalling 81,555 NIM Contact EMG endotracheal tubes worldwide due to reports of airway obstruction during use.

    Product
    NIM CONTACT EMG Endotracheal Tube, Part Numbers: a) REF 8229508 b) REF 8229507 c) REF 8229506
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1615-2022·2022-09-07

    Lyons Barista Style Almond Beverage Recalled for Potential Bacterial Contamination

    Lyons Magnus is recalling Lyons Barista Style Almond non-dairy beverage nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Consumers should not consume the affected products.

    Product
    Lyons Barista Style Almond, Non-Dairy Beverage. Plant-Based Milk. 32 FL OZ (1 QT) 946mL UPC 0 45796-10165 4. 12 count case UPC 10045796101651. Shake Well before Serving. After opening keep refrigerated and use within 7 days. Lyons Magnus, Fresno, CA 93702.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1617-2022·2022-09-07

    Lyons Barista Oat Beverage Recalled for Potential Bacterial Contamination

    Lyons Magnus is recalling Lyons Barista Style Oat, a plant-based milk beverage distributed nationwide, due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.

    Product
    Lyons Barista Style Oat, Non-Dairy Beverage. Plant-Based Milk. 32 FL OZ (1 QT) 946mL UPC 0 45796-10180 7. 12 count case UPC 10045796101804. Shake Well before Serving. After opening keep refrigerated and use within 7 days. Lyons Magnus, Fresno, CA 93702.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1647-2022·2022-09-07

    Plant-based protein shake recalled for Cronobacter and botulinum contamination

    Lyons Magnus is recalling nationwide its Lyons Ready Care Plant-Based Protein Shake due to findings of and potential for Cronobacter sakazakii and Clostridium botulinum contamination. Affected lot codes are 5221 (08/08/2022) and 6221 (08/09/2022).

    Product
    Lyons Ready Care Plant-Based Protein Shake Vanilla. 8.45 fl oz. ( 250mL)UPC 0 45796-10080 0. Mildly Thick Nectar Consistency. Refrigerate prior to serving. Shake well. Sold in 24-count case UPC 10045796100807. Lyons Magnus, Fresno, CA 93702.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1521-2022·2022-09-07

    NIM EMG Endotracheal Tubes recalled for risk of airway obstruction

    Medtronic Xomed is recalling NIM EMG Endotracheal Tubes due to reports of airway obstruction during use. The recall affects 23,820 units distributed worldwide.

    Product
    NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229307J b) REF 8229308J c) REF 8229306J
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1620-2022·2022-09-07

    Plant Protein Drink Recalled for Potential Bacterial Contamination

    Lyons Magnus recalled pirq Plant Protein Super Foods drink due to potential Cronobacter sakazakii and Clostridium botulinum contamination. Consumers should not consume the product.

    Product
    pirq Plant Protein Super Foods, Golden Vanilla Drink, Almonds, Curcumin, Maca. 11 FL OZ (325ML). UPC 8 57690-00804 1. Packaged in the following configurations: 1. 12 count case UPC 857690008157. 2. 4 count wrap UPC 857690008256. Chill it, Shake it. Do not Fr
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V550000·2022-09-07

    2020-2021 Bentley Continental GT Front Seat May Trap Rear Passenger Legs

    Bentley is recalling certain 2020-2021 Continental GT vehicles because the front seat may trap a rear passenger's legs during automated movements. The front seat software will be updated free of charge.

    Product
    BENTLEY — 2021 BENTLEY CONTINENTAL GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1465-2022·2022-09-07

    Colgate OPTIC WHITE PRO Series Toothpaste Recalled for Improper Storage

    Family Dollar Stores is recalling 1,120 packages of Colgate OPTIC WHITE PRO SERIES toothpaste due to improper temperature storage conditions that deviate from cGMP standards.

    Product
    Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE PRO SERIES, Stain Prevention, 5% Hydrogen Peroxide, Net Wt. 2.1 OZ. (59 g) UPC 0 35000 99658 9. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1645-2022·2022-09-07

    X-Ray Imaging System X-Ray Tube Hardware Defect Worldwide Recall

    Siemens has recalled Artis Q and Artis Q.zen X-ray imaging systems due to a potential X-ray tube hardware defect. In rare cases, if error detection fails, the system will not be able to release X-ray until shut down; 1,389 units are affected globally.

    Product
    Artis Q floor- Model No. 10848280 Artis Q ceiling- Model No. 10848281 Artis Q biplane- Model No. 10848282 Artis Q zeego- Model No. 10848283 Artis Q.zen floor- Model No. 10848353 Artis Q.zen ceiling- Model No. 10848354 Artis Q.zen biplane- Model No. 10848355
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1468-2022·2022-09-07

    Colgate Anticavity Fluoride Toothpaste Recalled for Improper Storage Conditions

    Family Dollar is recalling Colgate OPTIC WHITE CHARCOAL COOL MINT toothpaste (Net Weight 4.2 oz., UPC 0 35000 97872 1) distributed to stores in 11 states due to improper temperature storage during manufacturing.

    Product
    Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE with CHARCOAL COOL MINT PASTE, Net Wt. 4.2 OZ. UPC 0 35000 97872 1. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1666-2022·2022-09-07

    Radiographic imaging system may exceed radiation dose limits in biplane mode

    Canon Medical's Alphenix i imaging systems may deliver radiation dose rates exceeding acceptable limits during biplane fluoroscopic procedures. Sixteen systems nationwide with software versions 8.0, 9.0, or 9.2 and TFP 1200C detector are affected.

    Product
    INFX-8000V. For radiographic and fluoroscopic studies and intervention.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1648-2022·2022-09-07

    Siemens Dimension Vista CA 15-3 Diagnostic Cartridges Recalled for Measurement Bias

    Siemens Healthcare Diagnostics is recalling Dimension Vista CA 15-3 Flex reagent cartridges because the diagnostic test can produce inaccurate results, reading 26–33% lower than actual values, potentially delaying appropriate patient treatment decisions.

    Product
    Dimension Vista LOCI CA 15-3 Flex reagent cartridge. In Vitro Diagnostic for the quantitative measurement of CA 15-3. Siemens Material Number (SMN)/Ref Catalog Number : 10464344/K6456
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1647-2022·2022-09-07

    Siemens Artis icono X-Ray Systems Recalled for Potential Hardware Failure

    Siemens has recalled Artis icono X-ray imaging systems due to a potential hardware issue affecting a specific lot of X-ray tubes. If the error detection mechanism fails, the system cannot release X-rays until it is shut down.

    Product
    Artis icono biplane- Model No. 11327600 Artis icono floor- Model No. 11327700
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1660-2022·2022-09-07

    ARCHITECT STAT Troponin-I Reagent Kit Recalled for Insufficient Blocking Agents

    Abbott is recalling one lot of ARCHITECT STAT Troponin-I Reagent Kits due to insufficient heterophilic blocking agents in the conjugate, which may affect test accuracy.

    Product
    ARCHITECT STAT Troponin-I Reagent Kit, REF 2K41-27
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1685-2022·2022-09-07

    Sucrose solution vials recalled nationwide for contamination and leaking

    Clinical Innovations is recalling Sweetums 24% sucrose solution vials due to reports of leaking containers and contamination with black liquid and particulates. The product is used in hospital settings including neonatal intensive care units.

    Product
    Sweetums 24% sucrose solution with preservative. Vials containing 1ml or 2ml of 24% sucrose in purified water. Product is administered by drop using vials and tip allows controlled administration directly to tongue or buccal surface. Product is only used in the hospital setting
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1684-2022·2022-09-07

    Clinical Innovations Sweetums Sucrose Solution Vials Recalled for Contamination

    Clinical Innovations is recalling Sweetums 24% sucrose solution vials due to complaints of leaking, black liquid, and black particulates in product vials. The recall affects neonatal products distributed nationwide and internationally.

    Product
    Sweetums 24% sucrose solution preservative free. Vials containing 1ml or 2ml of 24% sucrose in purified water. Product is administered by drop using vials and tip allows controlled administration directly to tongue or buccal surface. Product is only used in the hospital setti
    Category
    Medical Device
    Distribution
    Distributed nationwide