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.
Biopsybell is recalling 10G Direct Working Cannulas labeled as sterile because they may not have been sterilized. The recall affects 50 units distributed in Mississippi and Kentucky.
Biopsybell S.R.L. is recalling 330 units of 10G Direct Single Access devices because they were labeled as sterile but may not have been sterilized.
WillowWood Global LLC is recalling 815 Alpha Interlock Suspension System Lanyard Bodies because a shorter dowel pin was used, which may cause the suspension cord to slip or come loose.
Trek is recalling Bontrager Satellite City bicycle pedals because they may fall off the crank arm, posing fall and injury hazards to riders.
Conagra Brands is recalling Udi Gluten Free Chocolate Zucchini Muffins due to the potential presence of plastic. Consumers should stop eating the product.
Desserts On Us, Inc. is recalling 120 units of Original Pistachio Traditional Baklava because the packaging failed to declare milk as an ingredient.
Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters due to defects in the distal connector that may prevent proper catheter passage or locking.
Biopsybell is recalling 40 units of 10G coaxial cannulas labeled as sterile but potentially not sterilized. The units were distributed in Mississippi and Kentucky.
Agri Exim INC. is recalling Waah Organic Rajma Masala because it contains undeclared milk in the ghee ingredient.
RaySearch Laboratories is recalling RayStation and RayPlan software versions due to a defect that may mislabel approximate radiation doses as clinical doses.
PepsiCo is recalling Evolve Vanilla Bean Plant-Based Protein Shakes because they contain undeclared soy. The recall covers 14,830 cases distributed nationwide.
Conagra Brands is recalling Udi Gluten Free Double Chocolate Muffins due to the potential presence of plastic.
Bard Access Systems is recalling specific Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.
Fresenius Medical Care is recalling 709 cases of Delflex Peritoneal Dialysis Solution because a 4.25% dextrose bag was found inside a 1.5% dextrose box.
Bard Access Systems is recalling specific Groshong NXT ClearVue catheters due to defects in the distal connector that may prevent proper catheter passage or locking.
W.L. Gore & Associates is recalling 61 Gore Viabil Biliary Endoprosthesis devices because a complaint reported a device appeared shorter than its labeled length.
Sun Pharmaceutical Industries is recalling CEQUA (cyclosporine) ophthalmic solution due to subpotent drug levels and the presence of particulates.
Faribault Foods is recalling O Organics Organic Chili Beans because the cans have compromised hermetic seals. Consumers should stop using the product.
Boston Scientific is recalling 27 units of the ELUVIA Drug-Eluting Vascular Stent System because some 6x40mm stents were incorrectly placed in 6x100mm packaging.
NOW Health Group is recalling 10,235 bottles of NOW 4x6 Acidophilus because foreign capsules were found in the product.
Faribault Foods is recalling S&W Organic Black Beans because some cans have compromised hermetic seals. Consumers should check their cans and return them for a refund.
Conagra Brands is recalling Udi Gluten Free Blueberry Muffins due to the potential presence of plastic. Consumers should check lot codes and stop eating the product.
KVK-Tech, Inc. is recalling 17,096 bottles of Hydrocodone Bitartrate and Homatropine Methylibromide tablets due to failed impurities and degradation specifications.
SigmaPharm Laboratories is recalling Asenapine sublingual tablets because they were manufactured with the wrong flavoring agent.
Nomax Inc. is voluntarily recalling 78 cartons of Dry Eye Test strips due to subpotent drug content. The FDA classified this as a Class III recall.