State
73,596 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, 873 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,131 (28%) are Severe.
Which agencies issued them
These figures cover only the 7,533 recalls whose distribution notice names Oregon specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Utz Quality Foods is recalling 2.0 oz bags of Dirty Sour Cream and Onion Potato Chips due to potential Salmonella contamination. The product was distributed across 32 US states.
Utz Quality Foods is recalling 2.0 oz bags of Dirty Maui Onion Chips due to potential Salmonella contamination. The product was distributed across 32 US states.
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance. The recall affects 113,843 kits distributed nationwide and in Barbados.
Spring & Mulberry Inc. is recalling Spring & Mulberry Coffee Date-Sweetened Chocolate bars due to potential Salmonella contamination. The affected product was distributed nationwide.
Medline Industries is recalling 22 models of Convenience Kits that contain Lidocaine Hydrochloride Injection and Bupivacaine Hydrochloride in Dextrose Injection due to quality issues found during an FDA inspection of the supplier.
CareFusion is recalling 178,000 ChloraPrep One-Step antiseptic applicators (Lot #4073005) nationwide due to potential non-sterility from fungal contamination and seal breaches from paper lidding wrinkles.
Spring & Mulberry Inc. is recalling Sea Salt Date-Sweetened Chocolate bars due to potential Salmonella contamination. Approximately 9,932 individual bars distributed nationwide are affected.
Spring & Mulberry Inc. is recalling Spring & Mulberry Mixed Berry Date-Sweetened Chocolate bars due to potential Salmonella contamination. The recall affects approximately 66,779 individual bars distributed nationwide.
Medline Industries is recalling Medline Convenience Kits (models DYNJ905503F and DYNJ905503G) that contain Arrow Kits with Lidocaine Hydrochloride Injection and Bupivacaine Hydrochloride in Dextrose Injection due to quality issues found during an FDA inspection of the supplier.
Acumed LLC is recalling Hexalob Screws of various sizes used with wrist fixation systems due to a manufacturing error that may cause the screws to break during use.
Surgify Halo 5.4 mm surgical burrs may break during bi-portal endoscopic spinal surgery. The FDA is recalling this device nationwide due to the potential breakage hazard.
Nissan is recalling 2026 Leaf vehicles because rear seat belt retractors may deactivate early, preventing child restraints from securing properly.
Sun Pharmaceutical is recalling Perampanel 6 mg tablets due to labeling mix-up where 10 mg tablets were found in bottles labeled as 6 mg. Patients should verify their bottles with their pharmacy or physician.
Surgify Medical OY is recalling Surgify Halo 5.4 mm Long surgical burrs due to potential breakage during bi-portal endoscopic spinal surgery. The defect could affect patient safety during the procedure.
Surgify Medical is recalling Surgify Halo 5.4 mm Medium surgical burrs due to potential burr breakage during bi-portal endoscopic spinal surgery. The device poses a risk of fragmentation that could complicate surgical procedures.
Surgify Halo 4.0 mm extendable surgical burrs may break during bi-portal endoscopic spinal surgery. The device is being recalled to prevent patient injury from burr fragments.
Surgify Medical is recalling Surgify Halo 5.4 mm Short burrs (Model 54.070.NVG.H1) due to potential breakage during bi-portal endoscopic spinal surgery. The hazard could affect patient safety during the procedure.
SURGIFY MEDICAL OY is recalling Surgify Halo 5.4 mm Extendable surgical burrs (Model 54.000.SEE.H1) due to potential for burr breakage during bi-portal endoscopic spinal surgery. The device has been distributed nationwide.
Chrysler is recalling 2026 Ram 1500 vehicles because headlight wiring may cause parking and daytime running lights to flicker or fail, reducing visibility.
Honda is recalling 2018-2020 Odyssey vehicles because water may enter the rearview camera, causing the image to fail to display in reverse.
Surgify Halo 5.4 mm surgical burrs may break during bi-portal endoscopic spinal surgery. The FDA has classified this as a Class II recall affecting devices distributed nationwide.
Surgify Medical is recalling the Surgify Halo 4.0 mm surgical burr because it may break during bi-portal endoscopic spinal surgery. The device is distributed nationwide.
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA 510(k) clearance. Affected kits were distributed nationwide and internationally.
Surgify Halo 4.0 mm Short burrs may break during bi-portal endoscopic spinal surgery, creating a potential hazard during the procedure. The FDA has classified this as a Class II recall affecting devices nationwide.
Surgify Medical is recalling the Surgify Halo 5.4 mm surgical burrs due to potential breakage during spinal surgery procedures.