State
73,566 recalls have nationwide distribution and so reach Oregon. 7,533 additional recalls listed Oregon specifically in their distribution scope.
Of the 7,533 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 2,128 (28%) are Severe.
Which agencies issued them
These figures cover only the 7,533 recalls whose distribution notice names Oregon specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mickey Truck Bodies is recalling certain 2017-2018 commercial trucks because the license plate light shines rearward instead of downward, potentially confusing other drivers.
La Paloma is recalling about 70 girls' nightgowns sold online from November through December 2020 because they fail to meet federal flammability standards for children's sleepwear, posing a burn hazard. No injuries have been reported.
Gramr is recalling about 92,135 Brushed Gold Tea Kettles because they can expel hot water and excessive steam during use, posing a burn hazard. The company has received 122 reports of the kettles expelling hot water or steam, including 18 reports of minor burn injuries.
General Motors is recalling certain 2021 Buick Enclave and Chevrolet Traverse vehicles due to potentially incorrect air bag calibration software that may affect frontal air bag deployment.
Plant Guru is recalling about 25,600 units of wintergreen, birch, and essential oil blend products because the packaging is not child-resistant despite containing methyl salicylate, which poses a poisoning risk if swallowed by young children.
Volvo Trucks North America is recalling one Watson and Chalin steerable lift axle suspension system because short screws may fail to engage locking nuts, creating a road hazard.
Certain 2021 Nissan Rogue vehicles have improperly welded upper tether attachment points in the rear seat. This defect prevents child safety seats from being properly anchored, increasing injury risk during crashes.
HMO Beverage Corp. dba Organic Gemini LLC is recalling Organic Gemini TigerNut Flour (27.5 lb bags) because the product may be contaminated with Salmonella. Consumers should not consume the affected product.
Alexander Dennis is recalling 2017-2020 Enviro 500 buses because a sealing washer defect may cause high-pressure fuel leaks, increasing fire risk.
Volkswagen Group of America is recalling 2000-2002 Audi A4, S4, and 2000-2001 TT vehicles because driver airbag inflators may absorb moisture, potentially causing improper deployment in a crash.
Natural Foods Inc is recalling BulkFoods.com brand dehydrated chopped celery in 1lb and 5lb bags due to potential Salmonella contamination. The affected product was distributed to multiple states.
Tiger Nuts is recalling Tiger Nuts Flour 2.2 lb boxes due to potential Salmonella contamination. The affected product was distributed in Oregon, Missouri, Kansas, and nationwide through e-commerce.
Daimler Coaches is recalling 530 Setra S407 and S417 coaches because a cracked engine flap hinge could cause the flap to detach, creating a road hazard.
Imperia Elita Vitaccino Coffee sachets are being recalled because they were marketed without FDA approval and contain pharmaceutical ingredients Sibutramine and Fluoxetine. All lots distributed nationwide are affected.
Windstone Medical Packaging is recalling Angio Pack surgical kits containing angio tubing with incomplete or insufficient welds that may fail during use. The recall affects 190 units; no injuries have been reported.
Medtronic is recalling CB10R55R5 perfusion system tubing packs due to insufficient or incomplete welds that could compromise device function. The recall affects five tubing packs distributed across nine U.S. states.
Medtronic recalls specific lots of HY8M63R4 Adult ECC Custom Perfusion System tubing packs due to potentially insufficient or incomplete welds, which could affect performance during surgical procedures.
Bard Peripheral Vascular recalls VENOVO Venous Stent System 9F due to reports that the proximal end fails to expand immediately upon deployment and remains connected to the delivery system.
Anodyne Surgical has recalled hydrodissection cannulas due to a possible yellowish-brown or greenish-brown residue on the tip. The affected devices were distributed in multiple US states and Canada.
Medtronic is recalling 14 tubing packs of its HY10J00R12 perfusion system due to insufficient or incomplete welds. The affected lot is 221227814 with a use-by date of August 28, 2022.
Medtronic is recalling specific lots of BB10R94R6 Custom Perfusion System tubing packs due to incomplete or insufficient welds. The defect may affect device performance during use.
Medtronic is recalling specific lots of BB11J14R2 Bridge Custom Perfusion System tubing packs due to incomplete or insufficient welds that may have occurred during manufacturing.
Covidien, LP is recalling a mechanical respiratory filter (Item 351/5979) due to potential deviations in ethylene oxide sterilization. The product was distributed worldwide and in multiple U.S. states.
Abbott's WorkMate Claris cardiac monitoring system (Model H700124) is being recalled due to a software error that may disable the system or turn the screen black. Nine units affected in Michigan, Kansas, Missouri, and Texas.
Medivators, Inc. recalls 1,381 cases of dialysate concentrate due to a manufacturing anomaly that may result in out-of-specification formulation. Affected lots may not function properly in hemodialysis treatment.