State
73,092 recalls have nationwide distribution and so reach Ohio. 11,753 additional recalls listed Ohio specifically in their distribution scope.
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.
Which agencies issued them
These figures cover only the 11,753 recalls whose distribution notice names Ohio specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The JM Smucker Company is recalling Great Value Cinnamon Rolls nationwide due to possible plastic pieces in the product. Consumers should not consume affected units.
Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to polychlorinated biphenyls found in similar devices.
Caire recalls 739 FreeStyle Comfort portable oxygen concentrators that may fail to recharge their batteries. The devices were distributed in the US, Puerto Rico, Israel, and Peru.
Major Pharmaceuticals is recalling Guaifenesin Dextromethorphan Syrup nationwide for specific lots that failed to meet impurity and degradation specifications. Consumers should contact their pharmacist if they possess affected lots.
Philips is recalling Vue PACS Diagnostic Viewer software versions 12.1.5 to 12.2.8.454 because a defect may cause incorrect ischemic map calculations, potentially leading to misdiagnosis.
Maquet Cardiovascular is recalling approximately 33,823 units of the Acrobat-i Vacuum Stabilizer System due to manufacturing deviations that compromised the sterile barrier. Sterility cannot be assured for the 2-year shelf life.
Hobbs Medical recalls Posi-Stop Injection Needles because manufacturing debris in the needle can block injection solution flow.
CAIRE FreeStyle Comfort portable oxygen concentrators may fail to recharge their batteries, potentially leaving patients without access to supplemental oxygen. Twenty-three units have been recalled.
Major Pharmaceuticals has recalled Guaifenesin Dextromethorphan Syrup due to failed impurity and degradation specifications. Three lot numbers were distributed nationwide.
Six CAIRE FreeStyle Comfort oxygen concentrators may fail to recharge their batteries, potentially affecting portable use of these medical devices. Caire, Inc. is recalling affected units worldwide.
Lupin Pharmaceuticals is recalling 357,414 bottles of Ramipril 10 mg capsules due to CGMP deviations where the active pharmaceutical ingredient was sourced from an unapproved vendor. The affected product was distributed to 30 wholesalers with potential nationwide distribution.
Safecor Health is recalling certain Vitamin B1 supplements due to manufacturing defects where blister card-foils are separating from the blister cavity.
Safecor Health, LLC is recalling 1,470 boxes of Aspirin 81 mg chewable tablets nationwide due to a manufacturing defect where blister card-foils are separating from the blister cavity.
Nestle Health Science is recalling Douglas Labs Stress-B-Plus Dietary Supplement due to incorrect formulation. The product contains Niacin as Nicotinic acid but the label states Niacinamide.
Padagis is recalling 10,872 jars of Triamcinolone Acetonide Cream USP 0.025% nationwide because some jars contain subpotent or superpotent active ingredient levels. The defect was discovered during long-term stability testing.
Safecor Health is recalling specific lots of Vitamin D3 25 mcg tablets due to a manufacturing defect where blister card-foils may separate from the blister cavity. No illnesses or injuries have been reported.
Safecor Health recalls 791 boxes of Calcium Carbonate chewable tablets (Lot 24A0073) due to cGMP deviations where blister card-foils separated from blister cavities.
Olympus is recalling 1,749 GIF-1TH190 gastrointestinal videoscopes to clarify drying procedures in the instructions for use after human errors were identified during evaluation.
Dr. Reddy's Laboratories is recalling ibuprofen 600 mg tablets for failed tablet specifications. The affected product was distributed nationwide.
GM is recalling certain 2024 Silverado HD and Sierra HD vehicles with power-unlatching tailgates because the gate-release switch may short circuit and unlatch the tailgate.
Volvo Bus is recalling 2025 9700 buses because emergency exit labels may detach, potentially delaying evacuation and increasing injury risk.
Maserati is recalling certain 2023-2024 Grecale and 2024 GranTurismo vehicles because park assist module software may prevent the rearview image displaying in reverse.
Winnebago is recalling certain 2024-2025 Ekko motorhomes because the wheel bolts for the spare tire may be missing. 632 units are affected.
Mitsubishi Fuso is recalling 2016-2020 FEC52, FEC72, and FEC92 trucks because the rear leaf spring may break, creating a road hazard.
Pagani is recalling 2024 Utopia vehicles because a dashboard defect may prevent the passenger air bag from deploying correctly, increasing injury risk.