State
20,305 recalls have nationwide distribution and so reach Oregon. 0 additional recalls listed Oregon 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 Oregon 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.
GlaxoSmithKline is recalling 67,508 Anoro Ellipta inhalers nationwide because coarse particle mass failed release testing and was found out of specification. No illnesses have been reported.
CARDINAL HEALTHCARE is recalling Amoxicillin for Oral Suspension nationwide due to CGMP deviations. Products were exposed to temperatures outside their labeled storage conditions.
Ricola Cherry Honey Herb Throat Drops are recalled because products in batch 2000058693 were exposed to temperatures outside the labeled storage conditions during distribution. The Class II recall affects nationwide shipments.
Cardinal Healthcare is recalling Citalopram 20mg tablets (batch 3131748) nationwide due to exposure to temperatures outside labeled storage conditions during manufacturing.
Cardinal Healthcare is recalling Aripiprazole 5 mg tablets nationwide due to CGMP deviations. Products were exposed to temperatures outside labeled storage conditions. No illnesses have been reported.
Steris Corporation recalls Medivators Advantage endoscope hookup accessories because identification labels become illegible as ink degrades, potentially preventing proper hookup identification and delaying patient procedures.
Lillow oral contraceptive tablets (batch A5921) have been recalled nationwide by Cardinal Healthcare due to exposure to temperatures outside labeled storage conditions.
Certain Liberty Select Cycler hemodialysis machines may display an incorrect timestamp on treatment data reports sent to clinics. No injuries or illnesses have been reported.
Cardinal Healthcare is recalling Meloxicam 15 mg tablets nationwide due to exposure to temperatures outside labeled storage conditions. No adverse events have been reported.
General Motors is recalling certain 2020-2024 Chevrolet Silverado and GMC Sierra pickup trucks due to faulty electronic tailgate switches that may inadvertently unlatch while the vehicle is parked. The defect can allow the tailgate to open while driving, potentially causing cargo loss and creating a road hazard.
Honda and Acura are recalling 750,114 vehicles from 2020-2022 model years. A defective front passenger seat weight sensor may fail to suppress the airbag, increasing the risk of injury in a crash.
Jayco is recalling certain 2020-2023 Entegra motorhomes because passenger seats may have improperly welded pedestals that can separate and cause the seat to loosen or detach.
Proterra is recalling certain 2020–2022 Catalyst and ZX5 buses due to windshield wiper motor failure. Inoperative wipers reduce visibility and increase crash risk.
Tiffin is recalling certain 2022–2024 Allegro Bay motorhomes because batteries may shift during travel, causing electrical arcing and fire risk. Dealers will install new hold-down hardware at no charge.
Hyundai is recalling 2023 IONIQ 5, IONIQ 6, and Genesis GV60 vehicles for rear driveshafts that may break under load due to improper heat treatment, causing loss of drive power. Dealers will replace the driveshaft free of charge.
ABS Remorques is recalling 2014-2023 RC, WC, LRC, and LWC semi-trailers due to coupling plate deterioration that may cause king pin failure and trailer detachment. Detached trailers cannot be controlled and may crash or obstruct traffic.
Certain 2021 Harley-Davidson motorcycles may not display the speedometer or neutral indicator at startup in freezing temperatures, creating a crash risk. Owners should contact Harley-Davidson for a free software update.
A set of 5mm magnetic balls sold online through Walmart.com via Joybuy is being recalled because the magnets are too strong and can cause serious internal injuries or death if swallowed, especially by children.
BlendJet Inc. is recalling approximately 4.8 million BlendJet 2 Portable Blenders because they can overheat, catch fire, or have blades that break off during use, creating fire and laceration hazards.
FNA Group is recalling about 2,930 Simpson Gas Pressure Washers with Electric Start because the lithium battery in the electric start system can overheat and pose a burn hazard. Two reports of battery overheating have been received, but no injuries have been reported.
Nurse Assist, LLC is recalling sterile water and saline bottles across multiple brands due to potential lack of sterility assurance. The products could be nonsterile and may cause infection.
Raw Seafoods Inc. is recalling frozen, lightly seasoned salmon burgers nationwide due to undeclared sesame seeds and milk, which pose serious allergic reaction risk to sensitive consumers.
ResMed is recalling the AirFit F30 Full Face Mask because the device contains magnets that can interfere with active medical implants and ferromagnetic objects. The original user guide did not adequately warn about safe distance requirements.
Nurse Assist recalls sodium chloride IV flush solutions due to potential loss of sterility assurance. Nonsterile solutions could cause infection when used for intravenous administration.
Insight Pharmaceuticals recalls TING 2% Miconazole Nitrate Athlete's Foot Spray due to benzene contamination. The recall affects 117,336 cans distributed nationwide and in Puerto Rico.