State
73,596 recalls have nationwide distribution and so reach Ohio. 11,764 additional recalls listed Ohio specifically in their distribution scope.
Of the 11,764 recalls naming Ohio we have scored against our rubric, 2,112 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,908 (25%) are Severe.
Which agencies issued them
These figures cover only the 11,764 recalls whose distribution notice names Ohio specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
5000 Years Foods is recalling White Whole Kimchi in 32 oz, 64 oz, and 128 oz glass jars due to potential Listeria monocytogenes contamination. The affected product was distributed through Illinois to retail locations potentially nationwide.
Edwards Lifesciences is recalling PediaSat Oximetry Catheter Kits due to potential internal leaks within the devices. The recall involves 218 units distributed across multiple U.S. states and internationally.
Pharmaceutical Associates Inc. is recalling Cimetidine Hydrochloride Oral Solution 300 mg/5 mL due to a lack of Current Good Manufacturing Practice (CGMP) and potential carryover of Senna Syrup.
Monfefo LLC is recalling Monfefo brand Turmeric Shot in 2oz glass bottles because the product was not manufactured according to specifications. Affected lots were distributed across multiple states.
The Prime TC-transport chair, designed for healthcare facility use, was distributed to residential customers who may not understand the professional-level operating instructions. The recall addresses potential risk of improper use by home users.
BMW is recalling certain 2022 X4 vehicles because the tire information label may contain incorrect tire size and pressure information. Installing wrong-sized or improperly inflated tires increases the risk of a crash.
Eli Lilly is recalling 36,540 vials of Zyprexa (olanzapine) 10 mg intramuscular injection due to manufacturing deviations affecting the drug product's appearance, size, and color.
Carl Zeiss Meditec is recalling 914 CIRRUS HD-OCT Model 6000 imaging devices. The manufacturer failed to obtain FDA pre-market clearance before selling the devices.
An Isolibrium Support Surface intended for healthcare facilities was distributed to home customers. While the labeling is correct, home users may not understand instructions intended for healthcare professionals.
Primark is recalling about 9,500 8-pack Scent Stamper Pens due to elevated levels of benzyl alcohol in the purple pen, which poses a risk of skin irritation. No injuries have been reported.
The FDA is recalling Kaluza C Flow Cytometry Software versions 1.0, 1.1.1, and 1.1.2 due to software anomalies that may generate erroneous results affecting diagnostic interpretation.
PAI Holdings is recalling Nystatin Oral Suspension nationwide due to a lack of Current Good Manufacturing Practice (CGMP) controls that could allow carryover of Senna Syrup into the product.
PAI Holdings is recalling Ethosuximide Oral Solution 250 mg/5 mL (Lot C9BC, expiration 31 October 2022) distributed nationwide due to potential carry-over contamination from Senna Syrup related to lack of current good manufacturing practices.
Medline Industries is recalling Total Knee convenience kits that may contain an expired saline irrigation solution component. The expired component may not maintain proper sterility for surgical use.
Aurobindo Pharma USA Inc. is recalling Sulfamethoxazole and Trimethoprim Tablets (800mg/160mg) due to potential metal contamination in the product. The recall affects approximately 3,800 bottles distributed nationwide.
Stryker's InTouch 2131 medical device, intended for healthcare facilities, was distributed to residential customers. Home users may not understand healthcare-specific instructions, creating a risk of improper use.
Zen Magnets and Neoballs high-powered spherical magnets are being recalled because swallowing multiple magnets can cause intestinal perforation, blockage, and death. About 10 million magnets sold individually and in sets since January 2009 are affected.
Kibbi, LLC is recalling 2018-2020 Renegade RVs because window vent adhesive may fail, posing a crash or injury risk.
Swab Wagon is recalling 2017-2019 Chevrolet and Ford medic vehicles because their LED lights are too bright, potentially blinding other drivers and increasing crash risk.
Cummins is recalling specific generator sets because lifting cables may be improperly crimped. This defect could cause the equipment to fall during lifting, increasing the risk of injury.
Kibbi, LLC is recalling 2019-2021 Renegade Vienna and Villagio recreational vehicles because exhaust heat may cause the storage box to melt or catch fire.
Newmar is recalling 2021-2022 motorhomes with Cummins L9 diesel engines due to a potential fuel leak from a fuel hose that could cause fire.
Alexis Fire Equipment is recalling 2015-2020 emergency vehicles because LED lights may be too bright, potentially affecting driver vision and increasing crash risk.
Ferrara Fire Apparatus is recalling one 2020 Igniter emergency vehicle because the instrument cluster display may lock up or become nonfunctional due to low voltage spikes.
Mercedes-Benz is recalling 2020 GLB 250 vehicles because air bag control software may prevent front seat belts and air bags from activating properly in a crash.