State

Ohio product recalls

72,940 recalls have nationwide distribution and so reach Ohio. 11,719 additional recalls listed Ohio specifically in their distribution scope.

What the numbers show

Total: 11,719
Critical: 2,106
Severe: 2,413
Most recent: 2026-09-09

Of the 11,719 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 2,413 (21%) are Severe.

Which agencies issued them

These figures cover only the 11,719 recalls whose distribution notice names Ohio specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5351–5375 of 84659

CriticalFDA (Food)·H-0630-2025·2025-10-01
Original Swiss cheese recalled over potential Listeria monocytogenes contamination
Middlefield Original Cheese Co-op Original Swiss Cheese, in 5 lb loaves and 2 lb deli bags with a sell-by date of 2/13/2026, is recalled for potential Listeria monocytogenes contamination.
Product
Middlefield Original Cheese Co-op Original Swiss Cheese, packaged as 5 lb. loaves wrapped in plastic and packed 2 loaves per case (distribution) or 8 loaves per case (retail), or sliced and packaged as 2 lb. deli bags and packed 5 bags per case
Category
Food
Distribution
4 states
CriticalFDA (Food)·H-0627-2025·2025-10-01
Shredded mozzarella and provolone recalled over potential Listeria monocytogenes contamination
Middlefield Original Cheese Co-op Shredded Mozzarella/Provolone Cheese, 5 lb bags with a sell-by date of 9/3/2025, is recalled for potential Listeria monocytogenes contamination. 7,455 lbs are affected.
Product
Middlefield Original Cheese Co-op Shredded Mozzarella/Provolone Cheese, 5 lbs., packaged in a plastic bag, packed 4 bags per case
Category
Food
Distribution
4 states
CriticalFDA (Food)·H-0028-2026·2025-10-01
Macaroni and cheese cartons recalled nationwide for undeclared cashew allergen
GOODLES is recalling 61,176 cartons of Here Comes Truffle creamy truffle flavored cheddar and shells because the product contains cashews that are not declared on the label.
Product
GOODLES HERE COMES TRUFFLE CREAMY TRUFFLE FLAVORED CHEDDAR AND SHELLS NET WT 6 OZ (170g) INGREDIENTS: GOODLES SHELLS (WHEAT FLOUR, CHICKPEA PROTEIN, WHEAT PROTEIN, NUTRIENTS EXTRACTED FROM [BROCCOLI, SPINACH, KALE, PUMPKIN, SWEET POTATO, SUNFLOWER SEED, CRANBERRY, CHLORELLA, MAIT
Category
Food
Distribution
37 states
CriticalFDA (Food)·H-0027-2026·2025-10-01
Plant-based white cheddar spirals recalled over undeclared milk allergen
GOODLES Vegan Is Believin' Plant-Based White Cheddar with Spirals, 5.25 oz, is recalled for undeclared milk. The FDA classified the action as Class I. 129,660 cartons are affected.
Product
GOODLES VEGAN IS BELIEVIN' PLANT-BASED WHITE CHEDDAR WITH SPIRALS NET WT 5.25 OZ (149g) INGREDIENTS: GOODLES SPIRALS (WHEAT FLOUR, CHICKPEA PROTEIN, WHEAT PROTEIN, NUTRIENTS EXTRACTED FROM [BROCCOLI, SPINACH, KALE, PUMPKIN, SWEET POTATO, SUNFLOWER SEED, CRANBERRY, CHLORELLA, MAIT
Category
Food
Distribution
37 states
CriticalFDA (Food)·H-0632-2025·2025-10-01
Monterey jack and provolone loaves recalled over potential Listeria monocytogenes contamination
Middlefield Original Cheese Co-op Monterey Jack and Provolone 5 lb loaves with a sell-by date of 2/13/2026 are recalled for potential Listeria monocytogenes contamination. 7,455 lbs are affected.
Product
1) Middlefield Original Cheese Co-op Monterey Jack, 5 lb., packaged as loaves wrapped in plastic and packed 8 loaves per case 2) Middlefield Original Cheese Co-op Provolone, 5 lb., packaged as loaves wrapped in plastic and packed 2 loaves per case
Category
Food
Distribution
4 states
CriticalFDA (Food)·H-0633-2025·2025-10-01
Shredded mozzarella cheese recalled over potential Listeria monocytogenes contamination
Middlefield Original Cheese Co-op Shredded Mozzarella Cheese, 5 lb bags with a sell-by date of 9/3/2025, is recalled for potential Listeria monocytogenes contamination.
Product
Middlefield Original Cheese Co-op Shredded Mozzarella Cheese, 5 lb., shredded in a plastic bag and packed 4 bags per case
Category
Food
Distribution
4 states
SevereFDA (Food)·H-0629-2025·2025-10-01
Middlefield Original Cheese Smoked Cheddar Recalled for Listeria Contamination
Middlefield Original Cheese Cooperative is recalling Smoked Cheddar 5 lb. loaves due to potential Listeria monocytogenes contamination. The recall affects products packed on August 14, 2025, distributed across OH, PA, WI, and TX.
Product
Middlefield Original Cheese Co-op Smoked Cheddar, 5 lb. loaves, packaged 8 loaves per case
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-2568-2025·2025-10-01
Automated Impella Controller units recalled for pump performance risk
Abiomed is recalling specific Automated Impella Controllers with defective Pump Driver Circuit Assemblies that may cause decreased pump performance or pump stop. The defect triggers Impella Failure or Impella Stopped Controller Failure alarms.
Product
Automated Impella Controller (AIC) with the below brands and product codes. Used with heart assist pump. 1. Impella Controller, Packaged, US; Product Code: 0042-0000-US. 2. Impella Controller, Packaged, US, Loaner; Product Code: 0042-0000-US-L. 3. Impella Controller, Package
Category
Medical Device
Distribution
17 states
SevereFDA (Food)·H-0625-2025·2025-10-01
Sunrise Creamery Dilly Pickle Monterey Jack Cheese recalled for Listeria
Middlefield Original Cheese Cooperative is recalling Sunrise Creamery Dilly Pickle Monterey Jack Cheese products due to potential Listeria monocytogenes contamination. Affected products were distributed in Ohio, Pennsylvania, Wisconsin, and Texas.
Product
1) Sunrise Creamery Dilly Pickle Monterey Jack Cheese with Dill Pickles, Net Wt. 6 oz., packaged individually in plastic, packed 12 per case, UPC: 810665011156 2) Sunrise Creamery Dilly Pickle Jack Monterey Jack Cheese with Dill Pickles, Net Wt. 1.25 LBS (567 g), packaged indivi
Category
Food
Distribution
4 states
SevereFDA (Food)·H-0628-2025·2025-10-01
Middlefield Cheddar Cheese Recalled Due to Listeria Contamination Risk
Middlefield Original Cheese Cooperative is recalling specific lots of All Natural Mild Cheddar Cheese and Shredded Cheddar Cheese due to potential contamination with Listeria monocytogenes.
Product
1) Middlefield Original Cheese Co-op All Natural Mild Cheddar Cheese, 5 lb., packaged as individual loaves wrapped in plastic, packed 2 loaves per case (distribution) or 8 loaves per case (retail) 2) Middlefield Original Cheese Co-op Shredded Cheddar Cheese, 5 lb., packaged in a
Category
Food
Distribution
4 states
SevereNHTSA·25V656000·2025-10-01
2025 Toyota Tacoma Driveshaft Defect Risks Steering Failure and Rollaway
Toyota is recalling certain 2025 Tacoma and Tacoma Hybrid vehicles because the front driveshaft CV joint may deform and break, impairing steering and risking vehicle rollaway while parked.
Product
TOYOTA — TOYOTA TACOMA, TACOMA HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V658000·2025-10-01
2026 Tesla Model Y: Reverse Lights May Fail to Illuminate
Tesla is recalling certain 2026 Model Y vehicles because the reverse lights may fail to illuminate due to a wiring defect, which could reduce visibility when backing and increase crash risk.
Product
TESLA — TESLA MODEL Y
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2626-2025·2025-10-01
Allura Xper FD20 systems recalled over component deterioration halting motorized movements
Philips Allura Xper FD20 systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 2,114 units are affected.
Product
Allura Xper FD20 Product Codes: (1)722012, (2) 722028, (3) 722006; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2604-2025·2025-10-01
CT 6000 scanners recalled because the patient table may drop unexpectedly
Philips CT 6000 systems, model 728307, are recalled because the patient support table may descend unexpectedly due to ball screw misalignment after a replacement. 6 units are affected.
Product
Philips CT systems labeled as the following: 1. CT 6000, Model Number: 728307.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2625-2025·2025-10-01
Allura Xper FD10 OR Table recalled over ageing power supply and drive
Philips Allura Xper FD10 OR Table systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 2 units are affected.
Product
Allura Xper FD10 OR Table Product Codes: (1)722022, (2) 722033; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2635-2025·2025-10-01
Allura CV20 systems recalled over internal component deterioration disabling motorized movement
Philips Allura CV20 systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 46 units are affected.
Product
Allura CV20; Product Code: 722031; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2632-2025·2025-10-01
Allura Xper FD20/10 systems recalled over deterioration disabling motorized movement
Philips Allura Xper FD20/10 systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 45 units are affected.
Product
Allura Xper FD20/10; Product Code: 722029; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2623-2025·2025-10-01
Allura Xper FD10 systems recalled over ageing internal components stopping motorised movement
Philips Allura Xper FD10 systems are recalled because deterioration of the CMOS battery, hard disk drive and/or power supply may make motorized movements unavailable. 1,117 units are affected.
Product
Allura Xper FD10 Product Codes: (1)722010, (2) 722026, (3) 722003; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V657000·2025-10-01
Toyota Tundra and Sequoia Hybrid rear visibility software defect recall
Toyota is recalling 2022-2025 Tundra, Tundra Hybrid, and 2023-2025 Sequoia Hybrid vehicles due to a software error that may prevent the rearview image from displaying when in reverse, reducing driver visibility and increasing crash risk.
Product
TOYOTA — TOYOTA TUNDRA HYBRID, TUNDRA, SEQUOIA HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2600-2025·2025-10-01
Ingenuity CT scanners recalled because the patient couch may descend unexpectedly
Philips Ingenuity CT systems are recalled because the patient support table may descend unexpectedly to its lowermost position due to ball screw misalignment after a replacement. 285 units are affected.
Product
Philips CT systems labeled as the following: 1. Ingenuity CT 728326, Model Number: 728321. 2. Ingenuity CT 728326, Model Number: 728323. 3. Ingenuity CT, Model Number: 728326.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2596-2025·2025-10-01
Brilliance 16 and 6 slice scanners recalled over patient table descent
Philips Brilliance 16 Power, Brilliance CT 16 Slice and Brilliance CT 6 Slice systems are recalled because the patient support table may descend unexpectedly after a ball screw replacement. 73 units are affected.
Product
Philips CT systems labeled as the following: 1. Brilliance 16 Power, Model Number: 728240. 2. Brilliance CT 16 Slice, Model Number: 728246. 3. Brilliance CT 6 Slice, Model Number: 728256.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2636-2025·2025-10-01
Vessel harvesting systems recalled after out-of-box failures in harvesting tool jaws
Vasoview Hemopro 3 Endoscopic Vessel Harvesting Systems are recalled after out-of-box failures including deformed jaw attachments, jaws not fully closed and lifted heater wire. 98 units are affected.
Product
Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIEW HEMOPRO 3 Endoscopic Vessel Harvesting (EVH) System (VH-6000, VH-6001, and VH-6010) is a vessel harvesting kit designed for use with a 7 mm endoscope to cut and cauterize vessel branches.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2595-2025·2025-10-01
Brilliance CT 40 and 64 channel systems recalled over unexpected couch descent
Philips Brilliance CT 40 Channel, Brilliance CT 64 Channel and Ingenuity Flex systems are recalled because the patient support table may descend unexpectedly after a ball screw replacement. 181 units are affected.
Product
Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel, Model Number: 728235. 2. Brilliance CT 64 Channel, Model Number: 728231. 3. Ingenuity Flex, Model Number: 728317
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2622-2025·2025-10-01
Patient monitors recalled over potential activation of an abnormal alarm pause
BeneVision N1 Patient Monitors are recalled because of the potential for activation of an abnormal alarm pause. 2,278 units are affected.
Product
BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017, 6660E-PA00014, 6660E-PA00012, 6660E-PA00011, 6660E-PA00018, 6660E-PA00015, 6660E-PA00020, Q6660E-PA00011, 6660E-PA00021, 6660E-PA00016, 6660E-PA00019, Q6660E-PA00018, 6660E-PA00010, Q6660E-PA00010, Q6660E-PA00021, Q
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2615-2025·2025-10-01
Orthopedic inserter adapters recalled over weld breakage between pin and holder
Ortoma Inserter Adapter OTD devices are recalled because of a weld breakage between the pin and the inserter holder. 261 devices are affected.
Product
Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight REF 30-201 Model Number: 2001 UDI-DI code: 07350137521019 Inserter Adapter OTD Pinnacle Straight REF 30-202 Model Number: 1001 UDI-DI code: 07350137520593 Reamer Adapter OTD REF 30-157 Model Number: 1003 UDI-
Category
Medical Device
Distribution
Distributed nationwide