State
72,940 recalls have nationwide distribution and so reach Ohio. 11,719 additional recalls listed Ohio specifically in their distribution scope.
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.
Rivian is recalling certain 2022-2025 R1T and 2022-2026 R1S vehicles because the bolts securing the second-row seat belt retractor assemblies may be improperly tightened.
Ford is recalling specific engine block heaters for 2013-2019 Ford and Lincoln vehicles because they may crack, leak coolant, and cause electrical short circuits that increase fire risk.
Gulf Stream is recalling 2026 Trail Boss and Ameri-Lite trailers because reversed taillight wires may cause turn signals to activate in the wrong direction.
About 25,000 Ruahouine Hair Growth Serum bottles are being recalled because the serum contains minoxidil and the packaging is not child-resistant.
About 170 R.X.Y adult bike helmets are being recalled because they do not comply with impact attenuation, positional stability, labeling and certification requirements.
About 6,100 Adams RealComfort and StyleWell Adirondack patio chairs are being recalled because the chairs can crack and collapse, posing injury and fall hazards.
About 95 Morgan Lane Asher Pajama Sets, Style 816TR in Petal, are being recalled because they violate the mandatory flammability standards for children's sleepwear.
About 11,900 BBWOO baby loungers are being recalled because the sides are too low, the foot openings are too wide, and the loungers have no stand.
About 4,100 Energizer Large Power Indicator Lanterns are being recalled because the lithium-ion batteries installed in them can overheat, posing a burn hazard.
About 1,260 Greatale self-feeding pillows are being recalled because they hold a bottle at an unsafe angle and fixed in place, which can lead to aspiration of milk or formula.
About 16,900 RootStim Beard Growth Serum bottles are being recalled because the serum contains minoxidil and the packaging is not child-resistant.
Ford is recalling certain 2016-2018 Focus, 2019 Explorer and 2024 Explorer vehicles because the engine block heater may crack and develop a coolant leak, causing a short circuit when plugged in.
About 1,500 KEAWIS crib mattresses are being recalled because they may not adequately fit certain play yards or non-full-sized cribs, creating gaps that pose an entrapment hazard.
About 1,320 HEZI brand power strips are being recalled because they have an ungrounded metal enclosure that poses an electrocution hazard if energized.
Ambriola is recalling 184 units of Locatelli Grated Pecorino Romano 48/8oz shippers after the product tested positive for Listeria monocytogenes.
MediNatura is recalling all lots within expiry of ReBoost Nasal Spray after the products were found to contain yeast, mold and microbial contamination identified as Achromobacter.
AVID Medical is recalling 52 Halyard Organ Recovery OR Packs because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.
Ambriola is recalling 964 bags of Locatelli Grated Pecorino Romano in 5 and 10-pound sizes after the product tested positive for Listeria monocytogenes.
AVID Medical is recalling 132 Halyard Organ Recovery OR Packs, kit code LLOG1000-15, because the devices are not suitable for organ transplant.
Ambriola is recalling 45 bags of Pinna Grated Pecorino Romano in 10-pound sizes after the product tested positive for Listeria monocytogenes.
Ambriola is recalling 179 bags of Ambriola Piccante grated Pecorino Romano in 5 and 10-pound sizes after the product tested positive for Listeria monocytogenes.
AVID Medical is recalling 380 Halyard Mini Plus Kit South units because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.
Ambriola is recalling 2,106 units of Boar's Head Grated Pecorino Romano in 6 oz cups after the product tested positive for Listeria monocytogenes.
Ambriola is recalling 1,015 bags of Sam's Pecorino Romano grated, 1.5 lb, after the product tested positive for Listeria monocytogenes.
Ambriola is recalling 405 five-pound bags of Boar's Head Pecorino Romano Grated after the product tested positive for Listeria monocytogenes.