The Recall Desk

State

Ohio product recalls

73,106 recalls have nationwide distribution and so reach Ohio. 11,753 additional recalls listed Ohio specifically in their distribution scope.

What the numbers show

Total
11,753
Critical
2,117
Severe
2,425
Most recent
2026-09-23

Of the 11,753 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 2,425 (21%) are Severe.

These figures cover only the 11,753 recalls whose distribution notice names Ohio specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

11901–11925 of 84859

  • SevereFDA (Food)·F-1335-2024·2024-06-12

    Sour Cream Stabilizer System Recalled for Potential Salmonella Contamination

    Danisco USA Inc. recalls Grindsted Sour Cream 6563 stabilizer system for potential Salmonella contamination affecting 33,600 kg distributed across the US, Canada, and Mexico.

    Product
    Grindsted Sour Cream 6563 non-GM Stabilizer System 20 kg/ 44.09 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1320-2024·2024-06-12

    Sweet roll dough blend recalled due to potential Salmonella contamination

    Danisco USA Inc. is recalling Grindsted Sweet Roll Dough Blend 2 Stabilizer & Emulsifier System due to potential Salmonella contamination. The product was distributed across the US, Canada, and Mexico.

    Product
    Grindsted Sweet Roll Dough Blend 2 Stabilizer & Emulsifier System 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1318-2024·2024-06-12

    Grindsted Creamer 2160 System Recalled for Salmonella Contamination

    Danisco USA Inc. is recalling Grindsted Creamer 2160 System bags due to potential Salmonella contamination. The recall affects 31,865.40 kg distributed across the US, Canada, and Mexico.

    Product
    Grindsted Creamer 2160 System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1327-2024·2024-06-12

    Avicel-plus Food Stabilizer Additive Recalled for Potential Salmonella

    Danisco USA Inc. is recalling Avicel-plus GP 1615 Stabilizer System FCC due to potential Salmonella contamination. The affected bulk food additive was distributed to manufacturers across multiple U.S. states, Canada, and Mexico.

    Product
    Avicel-plus GP 1615 Stabilizer System FCC, 1000 kg / 2204.62 bulk bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1305-2024·2024-06-12

    Danisco Germantown Stabilizer 1772-II Recalled for Salmonella

    Danisco USA Inc. is recalling Germantown Stabilizer 1772-II, a food stabilizer and emulsifier system, due to potential Salmonella contamination. The product was distributed across the U.S., Canada, and Mexico.

    Product
    Germantown Stabilizer 1772-II, Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1313-2024·2024-06-12

    Grindsted Stabilizer System Recalled for Potential Salmonella Contamination

    Danisco USA Inc. is recalling Grindsted CFF 1455 Stabilizer System due to potential Salmonella contamination. The product was distributed to commercial customers in 24 US states, Canada, and Mexico.

    Product
    Grindsted(R) CFF 1455 Stabilizer System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1317-2024·2024-06-12

    ASC 2138 Stabilizer and Emulsifier System Recalled for Salmonella

    Danisco USA Inc. recalls ASC 2138 Stabilizer and Emulsifier System due to potential Salmonella contamination. Affected product distributed across US, Canada, and Mexico.

    Product
    ASC 2138 Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·F-1333-2024·2024-06-12

    Danisco Grindsted Sweetlife Cinnamon Roll Stabilizer Recalled for Salmonella

    Danisco USA Inc. is recalling Grindsted Sweetlife CINN. Roll BAS Stabilizer & Emulsifier System due to potential Salmonella contamination. The product was distributed across 28 U.S. states, Canada, and Mexico.

    Product
    Grindsted Sweetlife CINN. Roll BAS Stabilizer & Emulsifier System, 22.68 kg/ 50 lb bag
    Category
    Food
    Distribution
    24 states
  • HighFDA (Devices)·Z-1960-2024·2024-06-12

    Vascular graft devices recalled due to slider component separation

    Atrium Medical is recalling ADVANTA VXT vascular grafts following complaints of separation between the slider component and swivel core.

    Product
    ADVANTA VXT, 7X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1294-2024·2024-06-12

    Blueberry Cream Cheese Spread recalled for potential Salmonella

    Schreiber Foods Inc is recalling 835,721 units of Essential Everyday Blueberry Cream Cheese Spread (8 oz) due to potential Salmonella contamination. No illnesses have been reported.

    Product
    Blueberry Cream Cheese Spread, Net Wt. 8 oz. (226g). Keep Refrigerated, packaged under the brand Essential Everyday, UPC 0 41303-04876 4. Distributed By UNFI, Providence, RI 02908.
    Category
    Food
    Distribution
    20 states
  • HighFDA (Devices)·Z-1969-2024·2024-06-12

    Vascular graft component separation: Atrium Medical ADVANTA VXT recall

    Atrium Medical is recalling ADVANTA VXT vascular grafts due to reported separation of the slider mechanism from the core component, which could compromise device integrity.

    Product
    ADVANTA VXT, 7X70, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1972-2024·2024-06-12

    Vascular Graft Component Separation Risk in ADVANTA VXT Models

    Atrium Medical Corporation recalled 53,308 ADVANTA VXT vascular grafts worldwide due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. Patients should consult their healthcare provider regarding appropriate follow-up care.

    Product
    ADVANTA VXT, 7X80, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1292-2024·2024-06-12

    Strawberry Cream Cheese Spread Recalled for Potential Salmonella Contamination

    Schreiber Foods Inc is recalling Strawberry Cream Cheese Spread sold under brands including Fareway, Happy Farms, Hy-Vee, and Schnuck due to potential Salmonella contamination. Approximately 835,721 units were distributed across multiple states and Puerto Rico.

    Product
    Strawberry Cream Cheese Spread, Net Wt 8 oz. (226g). Keep Refrigerated, packaged under the following brands: 1. Fareway, UPC 0 21333-83052 2. Packed for Fareway Store, Inc. Boone, Iowa 50036. 2. Happy Farms, UPC 4099100 101744, Dist & Sold Exclusively by Aldi, Batavia, IL…
    Category
    Food
    Distribution
    20 states
  • HighFDA (Devices)·Z-1935-2024·2024-06-12

    LOSPA Patella Knee Component Recalled for Unsupported Expiration Date

    CORENTEC's LOSPA Patella Component knee implants are recalled due to an unsupported 10-year expiration date. Thirty-five units were distributed nationwide.

    Product
    LOSPA Patella Component Model/Catalog Number: 01.10.9XX Software Version: N/A Product Description: Patella
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1999-2024·2024-06-12

    Vascular Graft Swivel Rod Separation Reported in ADVANTA VXT Devices

    Atrium Medical recalls ADVANTA VXT vascular grafts due to reported separation of the slider swivel rod from its core, creating a gap between components. No injuries reported.

    Product
    ADVANTA VXT, 4-7X45, 1GDS, CH, TPR-SW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1986-2024·2024-06-12

    Vascular graft component separation reported in Advanta VXT devices

    Atrium Medical Corporation recalls Advanta VXT vascular grafts due to separation of internal swivel components. Approximately 53,308 units worldwide are affected, with the slider GDS swivel rod potentially separating from its core.

    Product
    ADVANTA VXT, 6X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1937-2024·2024-06-12

    Medline Disposable Syringes Recalled for Inaccurate Volume Delivery

    Medline is recalling 25.2 million Luer Lock disposable syringes because testing documentation does not confirm they deliver accurate volumes across their claimed capacity. The inaccuracy may pose a risk to patient health.

    Product
    MEDLINE LUER LOCK DISPOSABLE SYRINGE WITHOUT NEEDLE, REF SYR101010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1993-2024·2024-06-12

    Vascular graft component separation reported in ADVANTA VXT devices

    Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. No injuries have been reported.

    Product
    ADVANTA VXT, 4-6X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2013-2024·2024-06-12

    FDA Recalls FLIXENE Vascular Graft Devices for Component Separation

    Atrium Medical Corporation recalls FLIXENE vascular graft devices due to reported separation of the Slider GDS Swivel Rod from its core, which could affect device function.

    Product
    FLIXENE, 4-7X35, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2000-2024·2024-06-12

    Vascular Graft Recalled Due to Potential Component Separation Risk

    Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to complaints of separation of the Slider GDS Swivel Rod from the Swivel Core. Over 53,000 units have been distributed worldwide.

    Product
    ADVANTA VXT, 4-7X80, 1GDS, FH, TPR-TW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1995-2024·2024-06-12

    Vascular Graft Component Separation Recall - Atrium Medical ADVANTA VXT

    Atrium Medical Corporation is recalling the ADVANTA VXT vascular graft due to reported separation of the Swivel Rod from the Swivel Core. The component separation poses a risk of device failure.

    Product
    ADVANTA VXT, 5-8X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1983-2024·2024-06-12

    Vascular graft separation defect recalled by Atrium Medical

    Atrium Medical is recalling ADVANTA VXT vascular grafts due to reported separation of internal components. The defect affects over 53,000 units distributed worldwide.

    Product
    ADVANTA VXT, 6X50, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1293-2024·2024-06-12

    Schreiber Foods Chive and Onion Cream Cheese Spread Recalled for Salmonella Risk

    Schreiber Foods is recalling Chive and Onion Cream Cheese Spread sold under the Fareway, Happy Farms, and Hy-Vee brands due to potential Salmonella contamination. Affected consumers should not consume the product.

    Product
    Chive and Onion Cream Cheese Spread, Net Wt. 8 oz. (226g). Keep Refrigerated, packaged under the following brands: 1. Fareway, UPC 0 21333-83066 9. Packed for Fareway Store, Inc. Boone, Iowa 50036. 2. Happy Farms, UPC 4099100 101751. Dist & Sold Exclusively by Aldi, Batavia, IL…
    Category
    Food
    Distribution
    20 states
  • HighFDA (Devices)·Z-1953-2024·2024-06-12

    Vascular Graft Device Recalled for Slider Component Separation

    Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reported separation of the slider component from the swivel core. The recall affects 53,308 units worldwide.

    Product
    ADVANTA VXT, 8X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1989-2024·2024-06-12

    ADVANTA VXT Vascular Graft Recalled for Swivel Rod Separation Risk

    Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts after reports of separation between the Slider GDS Swivel Rod and Swivel Core. This structural defect could affect device performance.

    Product
    ADVANTA VXT, 6X80, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide