State
72,966 recalls have nationwide distribution and so reach Oregon. 7,526 additional recalls listed Oregon specifically in their distribution scope.
Of the 7,526 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 7,526 recalls whose distribution notice names Oregon specifically. The 72,966 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Carvedilol Tablets USP, 12.5 mg, packaged by Major Pharmaceuticals, lot T05693, are recalled nationwide because N-Nitroso Carvedilol Impurity-1 exceeded the FDA-recommended 4.0 ppm limit. 26,628 cartons are affected.
Bayonet Luer-Lock injection needles, models 50-353-23 and 50-345-23, are recalled because affected product showed elevated cytotoxicity values, which may present a risk of intolerance or allergic reaction.
Hospira 8.4% Sodium Bicarbonate Injection USP, 50 mEq/50 mL, lot LH2671, is recalled nationwide for lack of assurance of sterility. 15,750 vials are affected.
Hospira Epinephrine Injection USP, 1 mg/10 mL, lots LY3681, LY4360 and LY4416, is recalled nationwide for lack of assurance of sterility. 49,620 vials are affected.
Cipla Albuterol Sulfate Inhalation Aerosol, 90 mcg, lot 4IB0519, is recalled nationwide after out-of-specification particle size distribution results at the 12-month stability point. 20,352 packs are affected.
Clearview Strep A Exact II Dipstick Respiratory Kits are recalled because a classification error in the inventory system sent devices to customers without the required license to buy them. 5 kits are affected.
DRS Vascular is recalling 264 Q-Stop Suture Retention Devices. The FDA enforcement record for this action carries a placeholder in place of a stated reason for the recall.
VITROS Chemistry Products Ca Slides, catalog number 145 0261, generations 67 and above, are recalled because calibration failures on VITROS XT systems delay calcium test results. 174,215 units are affected.
Tavaborole Topical Solution 5%, 10 mL bottles from lot T401968, distributed by Viona Pharmaceuticals, is recalled because of discoloration. 3,960 bottles are affected.
Sensodyne Pronamel Active Shield toothpaste is recalled for a label mix-up: the outer carton reads Fresh Mint while the tube reads Cool Mint/Whitening. The toothpaste inside is Fresh Mint, as the carton states.
Forest River is recalling certain 2018-2026 Riverstone fifth wheel trailers because the steel hydraulic brake lines may fail and leak brake fluid, causing a loss of brake function.
Polestar is recalling certain 2025 Polestar 3 vehicles because the hood wing front bumper may be missing bolts, allowing the bumper to detach and become a road hazard.
Tiffin Motorhomes is recalling 2025 GT1 Touring vans because rear seat belt buckles may be too short to fasten, increasing injury risk in a crash.
Chrysler is recalling specific Mopar rearview camera modules because cracks in the microprocessor may prevent the image from displaying properly, increasing crash risk.
Forest River is recalling 2026 Cedar Creek recreational trailers because they may lack an emergency exit window, posing a risk of injury during an emergency.
Chrysler is recalling certain 2019-2021 Ram ProMaster and 2019-2020 Dodge Journey vehicles because cracks in the microprocessor may stop the rearview camera image displaying properly.
Nova Bus is recalling 2013 LFS transit buses because coolant hoses may leak hot liquid into the passenger area, posing a burn risk.
Hyundai is recalling certain 2025–2026 Tucson and Santa Fe vehicles because engine connecting rod bolts may have been improperly tightened, risking loss of drive power, engine damage, oil leaks, and potential fire.
Kia is recalling certain 2025 K4 and Sorento vehicles because the connecting rod bolts in the engine may have been improperly tightened, which can cause a loss of drive power.
Keystone RV Company is recalling 2026 Springdale and Hideout travel trailers because pivot brackets on the bunk bed may bend or break, posing a risk of injury.
Truck Certification Services is recalling specific Load Carrying Capacity labels where weight units may be reversed, potentially leading to vehicle overloading.
ZF North America is recalling specific steering columns because improperly tightened bolts may cause steering components to separate, increasing the risk of a crash.
Ford is recalling specific Edge and Lincoln MKX vehicles because the rear brake jounce hose may rupture, causing a brake fluid leak that increases stopping distance.
Forest River is recalling certain 2024-2026 East to West Entrada recreational vehicles because an incorrectly wired 7-way harness may cause the trailer brakes to lock up when the RV brakes are applied.
New Flyer is recalling certain 2012-2025 Xcelsior buses that may have been built without enough emergency exits, or with exits in an incorrect location. This fails FMVSS 217.