State
20,371 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.
Polaris Industries is recalling about 2,300 Model Year 2022 PATRIOT BOOST RMK KHAOS and PATRIOT BOOST PRO RMK snowmobiles because the primary clutch bolt can break, causing clutch components to separate and create a projectile hazard.
Huffy Corporation is recalling about 28,550 Blue's Clues Foot to Floor Ride-on Toys because the toy can tip forward when young children ride it, causing falls and injuries. The company has received 19 reports of children falling forward, resulting in 18 facial injuries.
Trek is recalling Model Year 2022 Speed Concept SLR bicycles, MY 2021-2022 Emonda SLR bicycles, and MY 2020-2021-2022 Bontrager Aeolus RSL VR-C aftermarket handlebar stems because carbon handlebars can crack, posing fall and crash hazards.
IKEA is recalling METALLISK Espresso Makers with stainless-steel safety valves because the units can burst and expel hot contents, causing burn and scald injuries. About 2,100 units sold in the U.S. are affected.
Navitas steel rolling chassis for utility vehicles are recalled because the throttle pedal can stick in the depressed position, creating crash and injury hazards. About 3,700 units distributed nationwide from June 2020 through April 2022 are affected.
About 190 Big Game Hunters Mud Kitchens are being recalled because the brass water tap contains lead levels that exceed federal safety limits. Lead is toxic if ingested by young children.
Epoch Everlasting Play is recalling about 8,200 Kidoozie My First Activity Desk Toys due to entanglement and entrapment hazards. A protruding knob can become entangled with clothing, and the handle opening poses a jaw entrapment risk to children under 18 months.
Wilbur's of Maine Milk Chocolate Covered Blueberries are recalled because the product contains undeclared almonds, posing a risk to consumers with almond allergies.
HeartWare HVAD System Batteries are being recalled due to electrical faults that may prevent the battery from powering the device controller, accepting charges, or maintaining charge. Approximately 19,616 batteries distributed worldwide are affected.
Stradis Medical recalls 850 surgical forceps (NARMD MEDICAL DEPOT Forceps, part ZZ-0701) due to potentially compromised sterile barriers. Healthcare facilities with these units should identify affected lot numbers and contact the manufacturer for guidance.
Stradis Medical is recalling NARMD MEDICAL DEPOT Kelly Straight forceps because the sterile barrier may be compromised. The recall affects 825 units distributed nationwide in South Carolina.
Micro Therapeutics is recalling Echelon-14 microcatheters whose outer carton packaging was exposed to a wet substance during transport, posing a risk to device sterility.
Zydus Pharmaceuticals recalls Fulvestrant Injection lot B200076 due to failed purity and stability specifications. Distributed nationwide; expiration January 31, 2024.
Family Dollar is recalling SKYN Original, Elite, and LS non-latex condoms due to improper storage. Products sold between May 1 and June 10, 2022 were not stored in temperature-controlled conditions.
Trinity Sterile's IV catheter dressing trays are mislabeled as latex-free despite containing natural rubber latex in component 94-7002, risking allergic reactions in latex-sensitive users.
Family Dollar is recalling BIOTRU Multi-Purpose Solution (4 oz, SKU 999009) due to improper temperature-controlled storage. Approximately 1,051 units were affected across US Family Dollar stores.
Family Dollar is recalling Veriquick Pregnancy Test 2CT kits (SKU 903756) sold from May 1 to June 10, 2022 due to improper storage outside temperature-controlled areas.
Nephron Sterile Compounding Center is recalling PF-Labetalol HCl Injection nationwide due to manufacturing deviations that create potential for cross-contamination. No illnesses have been reported.
Family Dollar's NEW SKIN Liquid Bandage was not stored in temperature-controlled conditions, potentially compromising product integrity. Affected units were sold nationwide during May through June 2022.
Crown Prince Quality Smoked Baby Clams (3 oz cans, UPC 0 73230 00853 5) are recalled due to detectable PFAS contamination. Approximately 211,716 cans distributed nationwide are affected.
Family Dollar is recalling CURAD First Aid Kits (SKU 999037) that were improperly stored without temperature control from April 30 to June 10, 2022. The temperature exposure may have degraded medications or compromised medical devices within the kits.
Nephron Sterile Compounding Center is recalling 294 bags of Trisodium Citrate 0.5% Solution IV bags due to potential cross-contamination from manufacturing deviations. The affected lots were distributed nationwide.
GS Saline Solution (12 fl oz) was not stored in temperature-controlled areas, risking contamination. The affected product was sold at Family Dollar stores nationwide from May 1–June 10, 2022.
Nephron Sterile Compounding Center is recalling 2,030 bags of injectable bupivacaine due to potential cross-contamination from manufacturing process defects. No illnesses have been reported.
Family Dollar is recalling Fixodent Org Cream denture adhesive (2.4oz and 0.75oz travel sizes) sold May-June 2022 due to improper storage in non-temperature-controlled areas. No illnesses reported.