State
72,820 recalls have nationwide distribution and so reach Ohio. 11,718 additional recalls listed Ohio specifically in their distribution scope.
Of the 11,718 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 2,412 (21%) are Severe.
Which agencies issued them
These figures cover only the 11,718 recalls whose distribution notice names Ohio specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Syera is recalling Space Astronaut LED Finger Lights sold on Temu because the button cell batteries can be easily accessed by children, posing a risk of serious injury or death if swallowed.
Toyota is recalling certain 2024 Tacoma hybrid and 2024-2025 Tacoma vehicles because their rear shock absorber assemblies may corrode and fail, potentially detaching the external oil reservoir and creating a road hazard.
International is recalling 2027 HV, HX, LT, MV, and RH trucks because a wiper nut may loosen, causing wipers to disconnect and reducing visibility.
KC Imports and Exports is recalling Laser & LED Light Mini Laser Pointer Keychains because button cell batteries can be easily accessed by children, posing a risk of serious injury or death.
Chrysler is recalling specific Mopar seat belt assemblies because the rear outboard belts may twist and fail to retract, increasing injury risk.
Volvo Trucks is recalling 2026-2027 VNL and VNR models because center roof marker lights may fail to illuminate, reducing visibility.
Chrysler (FCA US, LLC) is recalling certain 2023-2026 Alfa Romeo Tonale and 2023-2025 Dodge Hornet vehicles because the rear outboard seat belts may fail to retract properly.
ResMed is recalling Astral 100/150 ventilators because supercapacitor electrolyte leakage can damage the charger chip, trigger a fail-safe state, and interrupt ventilation therapy.
Windstone Medical Packaging is recalling 15 AMS medical convenience kits containing Elevaris Lidocaine HCl injection USP due to supplier quality issues reported by Elevaris Medical Devices Inc.
Medtronic Perfusion Systems is recalling EOPA Elongated One-Piece Arterial Cannula Model 77722 due to potential pinhole leaks in the wire-wound body during use.
Medtronic Perfusion Systems is recalling EOPA Elongated One-Piece Arterial Cannula (Model 77522) due to potential pinhole leaks in the wire-wound body during use.
Stryker GmbH is recalling Hoffmann II Carbon Connecting Rods (catalog 50796090) because they may crack after cleaning and sterilization. The FDA classified this as a Class II recall.
Instrumentation Laboratory is recalling Bar Code Reader (BCR) wands used with GEM Premier 5000 and 7000 systems because they may assign patient results to the wrong patient ID.
Rivian Automotive, LLC is recalling certain 2025-2026 R1S and R1T vehicles because the front turn signals may fail to illuminate or flash.
Instrumentation Laboratory is recalling GEM Premier 5000 portable blood analyzer systems because BCR wands may assign patient results to an incorrect patient ID. FDA classifies this as Class II.
Instrumentation Laboratory is recalling certain GEM Premier 5000 blood analyzer systems because the bar code reader wand may assign patient results to the wrong patient ID.
Philips is recalling certain CT scanners because the clinical scan may not start automatically after Bolus Tracking, which could require a patient rescan and expose them to additional radiation.
Mylan Pharmaceuticals is recalling one lot of Mycophenolate Mofetil for Injection, 500 mg/vial, because precipitate was found in the vials. The recall covers 5,688 vials distributed nationwide.
Windstone Medical Packaging is recalling 15 AMS spinal convenience kits, lot 230451, because they contain Elevaris Lidocaine HCl injection recalled for supplier quality issues.
Instrumentation Laboratory is recalling Bar Code Reader (BCR) wands used with GEM Premier 5000 and 7000 systems because they may assign patient results to the wrong patient ID.
Philips is recalling IQon Spectral CT systems because the clinical scan may not start automatically after Bolus Tracking, requiring manual triggering and potentially causing extra radiation exposure.
IsoTis OrthoBiologics, Inc. is recalling OsteoBallast and Ballast bone graft extenders because they may contain less demineralized bone matrix than intended.
Stryker GmbH is recalling Hoffmann II Carbon Connecting Rods (catalog 50796060) because they may crack after cleaning and sterilization. The recall covers all lots and about 9,658 units distributed worldwide.
Instrumentation Laboratory is recalling the GEM Premier 5000 portable blood analyzer system because bar code reader wands may assign patient results to the wrong patient ID. The recall affects 21 units distributed nationwide.
Stryker is recalling Hoffmann II Carbon Connecting Rods (catalog 50796040) because they may crack after cleaning and sterilization.