State
20,322 recalls have nationwide distribution and so reach Ohio. 0 additional recalls listed Ohio specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Ohio consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
Philips is recalling 2D Perfusion diagnostic imaging software due to signal processing errors that can produce inaccurate presentations, potentially affecting clinical decisions.
BD Kiestra InoqulA+ (software versions 5.1/5.1.1) fails to display plate information after processing in clinical laboratories, risking diagnostic delays or specimen recollection.
Beckman Coulter is recalling Access Free T3 reagent test kits (Catalog #A13422, Lot #233968) because approximately 15-20% of samples produce falsely elevated results that could lead to misdiagnosis and inappropriate thyroid treatment.
Medtronic is recalling 10 units of INFINITY Multi-Axial Screws distributed in the US and Canada because incorrect titanium material reduces gripping strength in affected lots.
Medtronic is recalling INFINITY spinal implant screws manufactured with incorrect titanium material. The defect reduces the screw's gripping strength, risking implant performance in critical spinal fusion surgery.
Compass Health Brands is recalling the REX Pressure Therapy System because the user manual incorrectly claims the device can prevent deep vein thrombosis, an indication for which the device was not FDA-cleared.
Medtronic recalled approximately 1414 SenSight Extension Tunneler Kits due to a manufacturing defect where dual carriers were machined on only one side, preventing use for passing two extensions simultaneously.
CVS-distributed earwax removal drops containing carbamide peroxide are being recalled because the active ingredient may degrade and become subpotent before the labeled expiration date, potentially leaving the product ineffective.
Ortho-Clinical Diagnostics is recalling VITROS Anti-SARS-CoV-2 Total N Antibody Calibrators used in COVID-19 testing due to incorrect calibrator levels in Assay Data Disks, which can delay patient test results.
Avanos Medical is recalling Ballard Oral Care Swabs (codes 12241, 12243, 12251) due to incorrect expiration date labeling. The recall affects 5,475 cases distributed worldwide.
Pro-Dex Inc is recalling 199 KLS E-Coupling Adapter devices due to incorrect Unique Device Identifier (UDI) and GTIN codes. The devices were distributed nationwide.
Bagno Milano is recalling about 3,600 children's robes sold online from June 2022 through March 2023 because they fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries.
Lucky Global is recalling about 30 Lelinta Multi-Purpose Kids Helmets sold online at Walmart.com because they do not meet federal safety standards for positional stability and may fail to protect children in a crash.
Taizhou Jiawang Trading Co. is recalling about 868 NewCosplay children's sleepwear garments sold on Amazon from November 2021 through April 2022 because they fail to meet federal flammability standards and pose a burn hazard.
Stanley Black & Decker is recalling approximately 2.2 million fiberglass sledgehammers because the head can loosen and detach during use, posing an impact injury hazard. The company has received 192 reports of detachment, including two reported injuries.
Davey Water Products is recalling about 1,060 DynaDrive Fresh Water Well Pumps because inadequate grounding can pose an electric shock hazard. One electrical shock has been reported in Australia; no incidents have been reported in the United States.
Changshu Lingshang Trading's NewCosplay children's sleepwear fails to meet federal flammability standards, posing a burn injury risk to children. About 110 units sold on Amazon from October 2021 through May 2022 are affected.
Lil Anglers is recalling approximately 78,500 children's fishing rods sold as Kid Casters No Tangle Combos because they contain lead levels that exceed the federal lead content ban. Lead ingestion can cause adverse health effects in young children.
Rollerblade USA is recalling about 13,400 Fury Inline Skates because the rear brake support can fracture or separate, reducing stability and increasing the risk of falls. No injuries have been reported to date.
Multiple brands of frozen organic strawberries are being recalled due to potential hepatitis A contamination. The recall affects products distributed across the United States.
Scenic Fruit Company is recalling Trader Joe's Organic Tropical Fruit Blend and related products distributed nationwide and regionally due to potential Hepatitis A contamination from Mexican strawberries. Five lot numbers with Best By dates from April to June 2024 are affected.
Frozen Organic Strawberries sold under multiple brands (Kirkland Signature, Trader Joe's, and others) are being recalled due to potential hepatitis A contamination. Do not consume; discard or return to retailer.
E S Foods is recalling 1,044,918 meal kits containing animal crackers distributed nationwide due to potential bronze metal shaving contamination. No illnesses have been reported.
Impossible Foods is recalling 128,029 cases of Impossible Chicken Nuggets nationwide due to potential wood contamination. The products should not be consumed.
Philips CombiDiagnost R90 X-ray systems (Model Numbers 709030 and 709031) may experience electrical fire in the main cabinet if exposed to overvoltage or power surge.