State
73,478 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 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Dole recalled 3-pound garden salads after harvest equipment tested positive for Listeria monocytogenes. Affected product codes begin with B, with best-by dates December 23, 2021–January 8, 2022.
Dole Fresh Vegetables is recalling Marketside 24 oz Classic Iceberg Salad due to Listeria monocytogenes found on harvest equipment used to prepare the product. Distribution included all US states and parts of Canada.
Dole Fresh Vegetables is recalling Kroger 24 oz Classic Garden lettuce salad because harvest equipment was found contaminated with Listeria monocytogenes. Consumers should not eat the affected product.
Dole Fresh Vegetables Inc is recalling Dole 13.25oz Country Ranch Kits after Listeria monocytogenes was detected in harvest equipment. Products have best-by dates from December 23, 2021 through January 8, 2022.
Dole Fresh Vegetables Inc recalled its 13 oz Southwest Salad Kit after Listeria monocytogenes was detected in harvest equipment used for the raw iceberg lettuce. The company is asking consumers not to consume the product.
Dole Fresh Vegetables is recalling Dole 24oz Value Size Garden Salad due to Listeria monocytogenes contamination found in harvest equipment. Best-by dates December 23, 2021 through January 8, 2022 are affected.
Dole Fresh Vegetables is recalling 12oz iceberg lettuce packages because harvest equipment was found to contain Listeria monocytogenes.
Daimler Trucks is recalling certain 2020-2022 Freightliner M2 trucks due to brake drum cracking that can cause brake failure and increase crash risk. All vehicles have been remedied.
RISE UP RED EDITION Capsules, 650 mg, have been recalled because they contain undeclared tadalafil, an ingredient found in FDA-approved male sexual enhancement products. The product is an unapproved drug and was distributed nationwide via Amazon Marketplace.
Dole Fresh Vegetables recalls 9.1 oz Peppercorn Ranch Chopped Kits due to Listeria monocytogenes found in harvest equipment. The affected products were distributed across Canada and the United States.
Dole Fresh Vegetables recalls Kroger American Blend lettuce due to Listeria found on harvest equipment. Affected products distributed across the US and Canada have best-by dates from December 22, 2021 to January 9, 2022.
Dole Fresh Vegetables Inc is recalling multiple sizes of Dole Garden Salad due to Listeria monocytogenes found in harvest equipment used during lettuce harvesting.
Dole Fresh Vegetables recalled Kroger 12 oz Classic Garden salad mix after Listeria monocytogenes was found in harvest equipment. Affected products have codes beginning with W and best-by dates from December 22, 2021 through January 9, 2022.
Dole Fresh Vegetables Inc is recalling 8oz packages of shredded lettuce because harvest equipment was found to contain Listeria monocytogenes. The recalled products have best-by dates from December 23, 2021 through January 8, 2022.
Dole is recalling certain Teriyaki Pineapple Kits due to Listeria monocytogenes detected in harvest equipment. Affected products have codes beginning with W and best-by dates from December 22, 2021 through January 9, 2022.
Biomet is recalling a Comprehensive Shoulder System implant component due to a defect in the porous plasma coating. The coating may not have sufficient adhesion strength, compromising the implant's structural integrity.
Keystone RV Company is recalling 2022 Crossroads Sunset 330SI travel trailers because the outside electrical receptacle may lack proper ground-fault protection, posing a shock risk.
BD's Vacutainer Luer Lok Access Device may release contaminant particles that can be misidentified as red blood cells in laboratory analysis, potentially leading to false elevated RBC counts.
Biomet is recalling 19 units of the Arcos Modular Revision Hip System because an incorrect rework process may have weakened the coating's adhesion strength, posing a potential implant failure risk.
Nobel Biocare is recalling 702 NobelReplace dental implant components due to a manufacturing defect that prevents proper driver engagement. The defect could result in aborted or delayed surgical procedures.
Petzl is recalling about 3,450 PIRANA descender canyoneering devices because the rope can get caught in the blocking slot, stopping or suspending the climber and creating a drowning risk under waterfalls or pools.
Collagen Matrix is recalling RESODURA matrix onlay dural substitutes due to outer packaging that is not properly sealed, potentially compromising sterility and creating a risk of infection.
Biomet recalls 9 Comprehensive Shoulder System Mini Humeral Stems due to potential coating adhesion defects. An incorrect rework process may have compromised the porous plasma coating adhesion strength.
Biomet is recalling a shoulder implant stem due to a manufacturing defect in the porous plasma coating. Internal testing indicated the coating may not have sufficient adhesion strength after an unvalidated waterjet rework process.
Natus Neurology is recalling IPELA FHD PTZ tile kits that may not fit properly in thinner ceiling tile grids and could suddenly fall, creating a safety hazard.