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.
About 2,015 Romorgniz fabric 12- and 13-drawer dressers are being recalled because they are unstable when not anchored to a wall and violate the STURDY Act standard.
Nissan is recalling certain 2025 Sentra vehicles because the windshield glass may have visible air bubbles, which can obscure the driver's visibility. This fails FMVSS 205.
Volvo Trucks is recalling certain 2024–2026 VNL (4) trucks because load lock clamps on the cab back may loosen, allowing cargo to shift or fall and create a crash hazard.
Mack Trucks is recalling 2025-2026 Pioneer and 2026 Anthem vehicles because automatic high beams may fail to switch to low beams, increasing crash risk.
Hyundai is recalling certain 2025 and 2026 vehicles because side curtain airbags may not have been installed properly and could fail to deploy in a crash. Dealers will reinstall the airbags free of charge.
About 70 play yards with a bear print are being recalled because infants can become entrapped under the mattress or between the mattress and the side.
About 2,100 Mallimoda children's pajama sets are being recalled because they violate the mandatory flammability standards for children's sleepwear.
Volvo Trucks is recalling certain 2024–2026 VNL and 2026 VNR trucks because their automatic high beam headlights may fail to switch to low beam, violating federal lighting standards and increasing crash risk.
Pacific International Marketing is recalling 308 cases of conventional Italian parsley over potential Salmonella contamination. The FDA has classified the recall as Class I.
Lotus Vaping Technologies is recalling Monarch Premium Kratom Green Maeng Da powder in three sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.
Lotus Vaping Technologies is recalling Monarch Premium Kratom Bali Gold powder in 4 oz and 8 oz sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.
JFE Franchising is recalling 177 units, 154.88 pounds, of 16 oz peach salsa in clamshells because the peaches supplied by Moonlight Peaches are potentially contaminated with Listeria.
Pacific International Marketing is recalling 2 cases of 30-count iceless conventional Italian parsley over potential Salmonella. The FDA has classified the recall as Class I.
Medline is recalling 96,406 breast and hernia convenience kits after complaints of anesthesia circuit leaks caused by cracks in the 120-inch expandable tubing. The FDA classified it Class I.
Medline is recalling ENT and laryngoscopy-bronchoscopy kits containing anesthesia circuits after complaints of leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.
Medline is recalling multiple adult 120-inch expandable anesthesia circuits after complaints of leaks caused by cracks in the tubing. The FDA has classified it Class I.
Cerenovus is recalling 12,004 CEREPAK Detachable Coil System units because the coils may fail to detach, which could result in hemorrhagic and ischemic stroke. The FDA classified it Class I.
Medline is recalling the latex-free Breathing Kit DYNJ10550 after complaints of anesthesia circuit leaks caused by cracks in the 120-inch expandable tubing. The FDA classified it Class I.
Medline is recalling the 120-inch latex-free ExtendFlex anesthesia circuit after complaints of leaks caused by cracks in the expandable tubing. The FDA has classified it Class I.
Medline is recalling ortho spine, total joint and kyphoplasty convenience kits after complaints of anesthesia circuit leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.
Lotus Vaping Technologies is recalling Monarch Premium Kratom Red Bali powder in three sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.
Pacific International Marketing is recalling 160 cases of bagged conventional Italian parsley over potential Salmonella. The FDA has classified the recall as Class I.
Medline is recalling open heart supplement and vascular kits containing anesthesia circuits after complaints of leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.
Pacific International Marketing is recalling 4 cases of iceless conventional Italian parsley over potential Salmonella contamination. The FDA has classified the recall as Class I.
Medline is recalling GYN Robotic and Robotic Prostate convenience kits after complaints of anesthesia circuit leaks caused by cracks in the 120-inch expandable tubing. The FDA classified it Class I.