State
72,984 recalls have nationwide distribution and so reach Ohio. 11,723 additional recalls listed Ohio specifically in their distribution scope.
Of the 11,723 recalls naming Ohio we have scored against our rubric, 2,107 (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 11,723 recalls whose distribution notice names Ohio specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Long-Haul 5L ATV fuel containers sold on Amazon.com lack required child-resistant closures, posing burn, fire, and poisoning risks to children. About 815 units sold from January 2023 through October 2024 are recalled.
Frito-Lay is recalling 1,295 bags of Tostitos Cantina Traditional Yellow Corn Tortilla Chips because milk was not declared on the label. Affected products were distributed across 13 states.
McLaren is recalling certain 2020-2025 vehicles because brake lines may be routed incorrectly, activating the brakes on the wrong side and possibly locking a rear wheel.
Draeger, Inc. is recalling 65,150 units of the VentStar Flex 220 breathing circuit due to the potential for cracks to form in the hose. A crack could affect gas delivery during anesthesia or ventilation procedures.
Draeger, Inc. is recalling Anesthesia Circuit Kit Flex 1 devices nationwide and internationally due to potential cracks in the breathing circuit hose that conducts anesthesia gases.
Draeger is recalling the Anesthesia Circuit Kit Flex EPA due to the potential for cracks to form in the breathing circuit hose. Approximately 13,620 units have been distributed domestically and internationally. Users should discontinue use of affected units immediately.
Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex 6 (Model MP02744) due to potential cracks forming in the breathing circuit hose. Approximately 293,660 units were distributed nationwide and internationally.
Draeger's ID Circuit Flex 220 breathing circuit for anesthesia machines may develop cracks in the hose. The recall affects 3,325 units distributed nationwide and internationally.
Draeger's Anesthesia Circuit Kit Flex 2 is recalled because of the potential for cracks to form in the breathing circuit hose. No injuries have been reported.
Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex (P)2 due to the potential for cracks to form in the breathing circuit hose. This FDA Class I recall affects approximately 9,250 units distributed domestically and internationally.
Stryker Corporation is recalling 182,344 Otopore Cylinder Standard outer ear dressings due to potential defects in blister seals that may compromise sterility. Bubbles in packaging seals indicate the sterile barrier is breached.
Stryker is recalling over 182,000 Nasopore nasal dressings due to potential bubbles in the blister seal that could compromise the sterile barrier. The affected units were distributed nationwide.
Hiab USA Inc. is recalling specific Waltco ZS-MK2 series lift gates because insufficient lubrication may cause the cylinder pin to seize, leading to lift gate failure and injury risk.
Nestle-USA recalls Lean Cuisine Butternut Squash Ravioli for potential wood-like foreign material. Approximately 50,611 cases distributed across 36 states are affected.
Ethicon Endo Surgery recalls ETHIBOND EXCEL surgical sutures worldwide due to curing issues with the silicone coating on the needles identified during manufacturing.
Stryker Corporation is recalling Nasopore nasal dressings due to potential breaches in packaging sterility seals that could compromise product sterilization. Approximately 182,344 units have been distributed nationwide.
Stryker Corporation is recalling 182,344 units of Hemopore nasal/sinus wound dressing due to potential packaging seal defects that could compromise sterility. A bubble on the blister seal may indicate the sterile barrier has been breached.
Stryker is recalling 182,344 units of Nasopore Standard nasal dressings nationwide due to potential bubbles in blister seals that may breach the sterility barrier and increase contamination risk.
Stryker Corporation is recalling Otopore Square outer ear wound dressings nationwide because sterile packaging seals may develop bubbles, indicating a potential breach of the sterile barrier. Consumers should stop using affected units and contact their healthcare provider.
Reichert, Inc. is recalling 122 units of the Phoroptor VRx Digital Refraction System Model 16241 due to an assembly defect that could cause the device head to become loose and potentially detach.
SeaBear Smokedhouse Alehouse Clam Chowder pouches are recalled nationwide due to potential seal failure that could allow Clostridium botulinum contamination. Consumers should not consume the product.
Biocon Pharma is recalling 2,184 bottles of Atorvastatin Calcium Tablets USP 40 mg nationwide. The product failed to meet required dissolution specifications, which may affect medication absorption.
Stryker Corporation is recalling 182,344 units of Nasopore FD nasal dressing nationwide due to potentially breached sterile seals that may allow product contamination.
Beckman Coulter is recalling certain DxC 500 AU Clinical Chemistry Analyzers due to a software defect that prevents calculated test results from being recalculated when constituent tests are rerun, potentially delaying patient result reporting.
Nestle-USA recalls Lean Cuisine Lemon Garlic Shrimp Stir Fry (10 oz) due to potential wood-like foreign material. Approximately 7,212 cases distributed across 37 states; check Batch Number 4214595511 (Best By September 2025).