State
72,919 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 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Patoolio Direct electric pressure washers are recalled because they lack an integral ground-fault circuit interrupter, posing shock and electrocution hazards. 2,066 units are affected.
Altec is recalling 2025-2026 AM Series Aerial Devices because the emergency stop switch may fail to cut power, increasing injury risk.
LED Finger Beam Lights are recalled because they contain button cell batteries that can be easily accessed by children, violating the mandatory safety standard for toys.
Chrysler is recalling 2026 Ram 2500 trucks because steering column modules may cause a loss of electronic stability control, increasing crash risk.
Arch Studio tea kettles sold at Macy's are recalled because the handle can detach during use when heated, posing a burn hazard. Three reports of the handle detaching have been received.
SpringFlower 5-in-1 Montessori Toy Sets are recalled because an airplane-shaped teething toy has tentacle ends that can pose a choking hazard to young children. About 21,900 units are affected.
Lil' Buddies Pet Laser Toys are being recalled over the button cell batteries they contain. Consumers are directed to keep them from children and dispose of the batteries safely.
BATOYAK USA electric pressure washers are recalled because they lack an integral ground-fault circuit interrupter, posing shock and electrocution hazards. 360 units are affected.
Fisher & Paykel gas ranges are recalled because the oven can experience delayed ignition, causing gas to accumulate and the oven door to open from combustion. One minor burn injury has been reported.
Zoliquex adult portable bed rails are recalled because users can become entrapped within the rail or between the rail and the mattress, posing a risk of death by asphyxiation.
Manik and Apex-branded ATX computer power supplies are recalled because they lack a permanent on-product label warning of shock and electrocution hazards if the unit is opened.
Medline is recalling a further group of NAMIC Angiographic Syringe lots because the rotating adaptor can unwind during use and disconnect from the manifold. 149,439 units are affected.
Fresenius Kabi USA, LLC is recalling certain batches of 0.9% Sodium Chloride Injection due to concerns regarding sterility assurance.
Medline is recalling right and left heart catheterization and angiography kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect. 79,843 units are affected.
Medline is recalling Minor Plastic-LF convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold.
Roush is recalling 1,217 2026 Nissan Frontier Pro4X R vehicles because steering and suspension fasteners may be loose or missing, posing a crash risk.
Medline is recalling custom manifold and cryo EP manifold kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use. 1,698 kits are affected.
Medline is recalling Delivery Pack convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold.
Medline is recalling Angio Pack and Neuro Interventional Radiology convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Medline is recalling Robotic Pack and Uro/Gen Robotic Pack convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Medline is recalling laparoscopic herniorrhaphy, lap and minor procedure packs containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Medline is recalling TAVR PACK convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold. 108 units are affected.
Medline is recalling NAMIC Angiographic Syringes across multiple sizes because the rotating adaptor can unwind during use and disconnect from the manifold. 1,752,096 units are affected.
Medline is recalling Head and Neck CDS-LF and Heart Cath Pack-LF convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect.
Medline is recalling cath lab and angiography procedure packs containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect. 17,902 kits are affected.