State
72,919 recalls have nationwide distribution and so reach Oregon. 7,525 additional recalls listed Oregon specifically in their distribution scope.
Of the 7,525 recalls naming Oregon we have scored against our rubric, 876 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,803 (24%) are Severe.
Which agencies issued them
These figures cover only the 7,525 recalls whose distribution notice names Oregon specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Leading Pharma, LLC is recalling Furosemide 80 mg tablets due to the presence of N-nitroso-Furosemide (NNF) above the recommended intake limit, caused by manufacturing deviations.
Integra LifeSciences is recalling the CUSA Clarity C7000 Console (Software Version 2.1.1.909) due to a software issue that renders the touch screen unresponsive during surgical use.
The FDA has rescinded regulatory clearances for certain Control Syringes, Guidewires, and High-Pressure Tubing included in Medline's Arthroscopy Pack (Model DYNJ82440). Affected units should not be used.
Arrow International is recalling 85 units of the Arrow Echogenic Introducer Needle due to incorrect manufacturing of the liquid adhesive used in the device.
Medline Industries has issued a recall of Medline Namic Guidewires because their FDA 510(k) regulatory clearances have been rescinded. The affected units were distributed nationwide.
Medline Industries is recalling Convenience Kits containing 10mL Polycarbonate Colored Syringes due to unapproved design changes made outside of FDA 510(k) clearance. The recall affects approximately 270,311 units distributed in the US and internationally.
Medline Industries has recalled multiple control syringes, guidewires, and high-pressure tubing models because their FDA 510(k) regulatory clearances have been rescinded. The recall affects 38,230 units distributed nationwide.
Medline Industries is recalling certain surgical and medical kits because their 510(k) regulatory clearances for Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. About 2,609 units were distributed nationwide.
Premier Dental Products is recalling Monsel's Solution (ferric subsulfate) 8 mL vials because the expiration date on the vial itself is printed with an extra digit (2709114 instead of 270914). The carton expiration date is correct.
Lode-King is recalling 2019-2026 trailers because missing welds on the rear impact guard reduce structural strength, increasing injury risk in rear-end crashes.
Ford is recalling certain 2024-2026 Ranger and Bronco vehicles because the front seat frame height-adjust pivot bolt may be loose or dislodged. 179,698 vehicles are affected.
Harley-Davidson is recalling certain 2024–2026 motorcycles with a potentially blocked airbox breather port that may cause crankcase pressure to build up, risking oil ejection and injury when the dipstick is removed.
Jayco is recalling 2026 Entegra Condor and Granite Ridge motorhomes because a tempering mixing valve may be missing from the water heater, creating a scalding risk.
American Battery Solutions is recalling Proliance High Voltage Batteries because a contactor may fail to close, causing a loss of drive power and increasing crash risk.
Audi is recalling certain 2025 Q5, Q5 Sportback, SQ5 and SQ5 Sportback vehicles because the driver and front passenger seat belts may have been manufactured incorrectly.
Shyft Group is recalling 2022 Utilimaster Aeromaster vehicles because the Gross Vehicle Weight Rating on the certification label may be incorrect, potentially leading to overloading.
AMZCMJ DGD is recalling its children's tower stools because they can tip over or collapse, posing risks of serious injury or death from falls and entrapment.
FitRx SmartBell Quick-Select adjustable dumbbells are recalled after more than 115 reports of weight plates dislodging during use, with at least six injuries including broken toes.
REV is recalling 2026 Fleetwood and Holiday Rambler motorhomes because a furnace defect may turn on the generator unexpectedly, posing a carbon monoxide risk.
32 Degrees heated socks sold at Costco are recalled after 14 heat-related incidents, 13 of them involving first- or second-degree burns. About 207,806 units are affected.
Mack Trucks is recalling 2,772 Pioneer and Anthem vehicles because unprotected electrical connectors may cause a loss of anti-lock brakes and stability control.
KMUYSL Big Red Barn Farm Animal Playsets are recalled because the fence handles can detach from a toy intended for children under three, violating the small parts ban.
BlissfulDestiny is recalling its Magnetic Stick Figure Sets because they contain loose magnets that pose a serious injury or death risk if swallowed.
TOETOL HOME children's tower stools are recalled because they can collapse or tip over and a child's torso can fit through the side openings. 18 collapses and 11 injuries reported.
Autobrush Sonic Pro Kids toothbrush delivery boxes are recalled because they contain a lithium coin battery that can be easily accessed by children, posing an ingestion hazard.