State
72,986 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 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
SHEIN Distribution Corporation recalls about 17,300 children's pajama sets sold on SHEIN.com between August 2023 and November 2024 for violating federal flammability standards for children's sleepwear, which poses a burn injury risk.
Chrysler is recalling certain 2021-2022 Jeep Grand Cherokee and Grand Cherokee L vehicles because a transistor in the centre stack display may overheat and blank the rearview image.
Rivian is recalling certain 2025 R1S and R1T vehicles because the headlight low beams may fail to illuminate when starting the vehicle in cold weather, failing FMVSS 108.
Toyota is recalling certain 2021-2025 Sienna Hybrid vehicles because the bolts for the third-row seatbacks may not be tightened properly. 167,802 units are affected.
About 4,400 Spritz Resin Hanukkah Dino Menorahs are recalled due to fire hazard. Target received 58 reports of the resin menorahs catching fire, scorching, charring, or melting when holding lit candles. No injuries reported. Return for full refund.
AFTCO is recalling about 820 Youth Solitude Jackets due to a strangulation hazard from the retractable drawstring in the hood. The drawstring can get caught on objects, posing a risk of serious injury or death to children.
Jaguar Land Rover is recalling 2020 Range Rover Evoque vehicles because the right-side lower knee air bag cover may come loose, potentially preventing proper deployment in a crash.
The 6-in-1 Pounding Game, sold on Temu.com, is recalled because a magnet in the wooden bird can break off and become an ingestion hazard for children.
Chrysler is recalling specific Mopar Center Stack displays because a transistor may overheat, preventing the rearview camera image from displaying and increasing crash risk.
Common Sense Soap is recalling approximately 33,899 pounds of beef tallow products produced without federal inspection. The products were shipped nationwide and lack a USDA mark of inspection.
La Fiesta PAN RAYADO Bread Crumbs are being recalled for undeclared sesame, an allergen not listed on the label. The recall affects 2,200 cases distributed nationwide.
Par Pharmaceutical is recalling Adrenalin Chloride Solution (Epinephrine Nasal Solution) due to a misleading label that resembles the FDA-approved Adrenalin epinephrine injection product, creating potential confusion.
La Fiesta Food Products is recalling seasoned bread crumbs because they contain undeclared sesame, an allergen not listed on the label. The product was distributed nationwide.
Terberg Benschop is recalling 2023-2024 YT Series vehicles because a steering arm bolt may be improperly tightened, risking loss of steering and a crash.
Porsche is recalling 878 2025 911 vehicles because a software error causes low beam headlights to create excessive glare for oncoming traffic, increasing crash risk.
GE Medical Systems is recalling Definium 656HD and Discovery XR656HD X-Ray systems due to an Automatic Exposure Control defect that may allow radiation exposure to exceed intended safety limits.
Philips is recalling AD7 and AD7X patient tables from Allura and Azurion fluoroscopy systems. During manual repositioning, fingers can become trapped between the guiding rails and tabletop, potentially causing injury.
SKY Packaging recalls Hydralazine Hydrochloride 25 mg tablets nationwide due to failed quality specifications for impurities and degradation.
Glenmark Pharmaceuticals is recalling carvedilol tablets nationwide due to N-nitroso carvedilol I (NNCI-I), a carcinogenic impurity found in certain lots. The impurity exceeds FDA safety limits.
Philips Azurion and Allura system patient tables may trap fingers between the guiding rails and tabletop during manual repositioning, risking finger injury to operators and service personnel.
The Philips AlluraXper FD20 operating room table can trap fingers between the guiding rails and tabletop during manual repositioning, potentially injuring operators and service personnel.
Ethicon is recalling PERMA-HAND Silk Sutures that may have open seals on packaging due to manufacturing defects, risking sterility compromise and patient infection. Approximately 78,792 units were distributed nationwide and internationally.
The Belmont Medical 3-Spike Disposable Set may leak during priming due to a crack in its female quick connector, potentially delaying warmed infusions in hospital settings.
GE Medical Systems' Discovery XR656HD X-Ray imaging systems can allow radiation exposures to exceed the Automatic Exposure Control limit without blocking further exposure. Approximately 3,149 units are affected worldwide, including 1,697 in the United States.
DDS Lab temporary titanium abutments may have been installed in some dental implant restoration cases instead of definitive abutments. The components may fracture, risking restoration loosening, oral tissue injury, and aspiration.