State
20,364 recalls have nationwide distribution and so reach Idaho. 0 additional recalls listed Idaho 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 Idaho 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.
Certain Toyota and Lexus vehicles may have a software defect preventing the Electronic Stability Control system from re-engaging after being manually disabled. Dealers will update the software free of charge.
NCH Life Sciences LLC is recalling hand sanitizer products containing excess acetal and acetaldehyde impurities due to manufacturing deviations. The recall affects 2.5 and 55-gallon bottles distributed nationwide in the US and Canada.
Acumed LLC recalled AcuTwist Acutrak Compression Screws (80,805 units) distributed without FDA pre-market clearance. The devices lack FDA evaluation for safety and effectiveness.
AVKARE LLC is recalling Glycopyrrolate 1 mg tablets distributed nationwide due to failed quality specifications involving unknown impurities. The recall affects 1,237 cartons.
Forest River is recalling certain 2021–2023 recreational vehicles because quick disconnect fittings in the LP gas system may crack and leak, creating a fire risk in the presence of an ignition source.
Acumed LLC is recalling Acutrak bone screws and fusion devices distributed without FDA pre-market clearance. Patients should contact their healthcare provider for guidance.
Acumed is recalling Acutrak 2 bone screw products distributed without FDA pre-market clearance. Healthcare providers should contact Acumed or the FDA for guidance regarding use and management of these devices.
Apotex Corp. is recalling Timolol Maleate Ophthalmic Solution 0.5% (lot TA4844) nationwide due to failed stability specifications showing excessive weight loss that may affect medication potency.
Shyft Group is recalling certain 2021-2022 Spartan RV Chassis K1-K4 vehicles. A steering column defect may cause the steering output shaft to disengage, resulting in loss of steering control and crash risk.
GM is recalling certain 2021 Chevrolet Tahoe vehicles because the second-row center seat belt latch may be trapped beneath the trim bezel. Passengers cannot use this seat belt, increasing injury risk in a crash.
General Motors is recalling certain 2017-2021 Chevrolet Camaro vehicles because the plastic 'Camaro' emblem on the steering wheel air bag cover may separate during air bag deployment, creating a projectile hazard.
Certain 2023 Mazda CX-50 vehicles with a trailer hitch may have a harness that detaches and becomes damaged, causing trailer lights and brakes to fail. This increases the risk of crashes when towing.
Airstream is recalling 2021-2023 travel trailers with SDS2 cooktops. Burner tubes may fracture and cause gas leaks, increasing fire risk. Dealers will install a support bracket at no charge.
Certain 2021 Ducati Multistrada V4 S motorcycles may have excessive valve guide wear that could break the valve head, decreasing engine performance and increasing crash risk. Ducati will replace the affected motorcycle engines at no cost.
Volkswagen is recalling 2021 ID.4 vehicles because a software defect in the battery management system may cause loss of drive power, increasing the risk of a crash. Free software updates will be provided by dealers.
ZLINE is recalling about 28,000 gas ranges because the oven can emit dangerous levels of carbon monoxide while in use, posing a serious risk of injury or death. The firm has received 44 reports of carbon monoxide emission, including three reports of consumers seeking medical attention.
Surf 9 is recalling Body Glove Tandem and ULI inflatable paddle boards sold at Costco because glue can separate at the seams, causing unexpected deflation and posing a drowning hazard. Three deflation reports have been received with no injuries yet reported.
Yamaha is recalling about 500 Viking Off-Road Side-by-Side vehicles because improper installation of parking brake retaining bolts could cause the brake to fail, allowing the parked vehicle to move unintentionally and potentially crash.
GE Vivid S6 N ultrasound systems may experience battery failure, smoke, or fire if batteries are not replaced every 2 years as recommended. Clinicians should replace batteries per manufacturer Service Manual instructions.
NuVasive's X-CORE 2 spinal implants may not disengage properly from the vertebral replacement device, potentially requiring revision surgery. About 2,031 devices worldwide are affected.
Baxter Healthcare Corporation is recalling 3.6 million Revaclear 400 Dialyzers due to a manufacturing defect where a twisted gasket could cause internal blood leaks during hemodialysis treatment.
Lupin Pharmaceuticals is recalling Quinapril 40mg tablets due to detection of N-Nitroso-quinapril impurity above acceptable daily intake limits. The recall affects approximately 30,612 bottles distributed nationwide.
Baxter Healthcare recalls Revaclear 400 Dialyzer units due to potential internal blood leaks caused by twisted gaskets. The defect may affect dialysis patients worldwide.
GE Medical Systems recalls Vivid i N ultrasound machines worldwide because unreplaced batteries may fail, emit smoke, or catch fire. Users should replace batteries every 2 years per the service manual.
Baxter is recalling approximately 14 million units of Revaclear 300 dialyzers worldwide due to polyurethane displacement that could cause blood leaks. No injuries have been reported.