State
20,199 recalls have nationwide distribution and so reach Washington. 0 additional recalls listed Washington 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 Washington 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.
CareFusion is recalling BD PYXIS MEDBANK medication dispensing cabinets due to a software issue that causes incorrect bin information to print on restock labels, potentially leading to medication selection errors.
The FDA is recalling 180 Leica HistoCore Arcadia H paraffin embedding stations due to a sealing defect in the paraffin tank that can cause toxic smoke and internal fire.
The BD PYXIS MEDBANK MINI automated dispensing cabinet software may print incorrect bin locations on restock labels, potentially causing medications to be placed in wrong locations.
Steris Corporation recalls certain automated endoscope reprocessor hookups due to incorrect instructions in product documentation. Improper hookup connection could prevent proper endoscope disinfection, risking patient infection.
Philips IntelliVue Patient Monitor models with software L.x and M.x lack critical monitoring capabilities due to a software update. This could result in incorrect or delayed patient treatment.
Philips IntelliVue Patient Monitors (MX400/450/500/550) with software versions L.x or M.x lack required monitoring capabilities due to removed software entitlements. The missing features could lead to incorrect or delayed patient treatment.
The Soltive Premium SuperPulsed Laser System may experience difficulties pairing its wireless footswitch, potentially delaying surgical procedures. The recall affects units distributed worldwide.
Olympus Corporation is recalling the Soltive Pro SuperPulsed Laser System due to difficulties pairing its wireless footswitch, which could delay surgical procedures. The recall affects 253 units worldwide.
Olympus Corporation of the Americas is recalling 1,838 units of the Soltive SuperPulsed Laser System Wireless Footswitch due to pairing difficulties that may delay surgical procedures.
A PEG-3350 oral solution is being recalled nationwide due to defective pouches that may not be properly sealed, risking product leakage. The recall affects 13,200 cartons with lot number S300542.
Amneal Pharmaceuticals recalls Methotrexate 2.5mg tablets (Lot BB29124) distributed nationwide due to potential presence of Fludrocortisone Acetate tablets. Patients should verify their lot number with their pharmacy.
Dr. Reddy's Laboratories is recalling Sevelamer Carbonate for Oral Suspension packets missing lot number and expiration date information. Approximately 5,136 cartons were distributed nationwide.
Lineage Biomedical is recalling NavaClick Syringe and Needle Model LIN02 due to an incorrect GTIN number on carton packaging. The recall affects 215 cartons distributed in Michigan and South Carolina.
Toyota is recalling 2022-2023 Corolla Cross vehicles where instrument panel defects may prevent the front-passenger air bag from deploying in a crash. Dealers will replace the panel at no cost.
Nova Bus is recalling 2023 LFS buses because the front air spring suspension hardware may separate from its attachment plate, potentially causing sudden loss of suspension and vehicle control.
Toyota and Lexus are recalling certain 2020-2022 vehicles with a faulty Occupant Classification System sensor that may prevent the front passenger air bag from deploying in a crash, increasing injury risk.
Audi is recalling 2019-2022 E-Tron vehicles because high-voltage battery modules may overheat and increase fire risk. Dealers will install diagnostic software and replace affected modules at no cost.
Audi is recalling certain 2023-2024 models because the driver's side airbag may be improperly mounted and fail to restrain occupants correctly in a crash.
Forest River is recalling 2021-2025 Impression fifth wheel travel trailers because the solar charge line, front LED hitch light, and pass-thru light may be wired to incorrect mini breakers, creating a fire risk.
CFMOTO is recalling certain 2022-2023 700CL-X motorcycles because ABS software may delay braking when the hand brake lever is squeezed multiple times, increasing crash risk. Dealers will update the software free of charge.
Ford is recalling 2024-2025 Escape vehicles with a defective passenger airbag cover that may prevent proper deployment, increasing injury risk and failing to meet federal safety standards.
Forest River and partner brands are recalling approximately 2,783 motorhomes with defective air conditioner soft start devices that may overheat and increase fire risk. Dealers will replace the devices at no charge.
Ford is recalling certain 2018-2025 Ford and Lincoln vehicles for missing air bag warning labels on the dashboard. The missing label increases risk of crash injury if occupants don't follow proper restraint guidelines.
Lion Electric is recalling certain 2024-2025 LionC school buses due to incorrect installation of anti-lock brake system pneumatic valve connections and rear wheel speed sensors, which can cause wheel lockup or loss of vehicle control.
General Motors is recalling certain 2023 Tahoe, Suburban, Escalade, Escalade ESV, Yukon, and Yukon XL vehicles due to improperly heat-treated rear suspension bolts that may break, risking wheel misalignment and crash.