State
72,940 recalls have nationwide distribution and so reach Oregon. 7,525 additional recalls listed Oregon specifically in their distribution scope.
Of the 7,525 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 7,525 recalls whose distribution notice names Oregon specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 300 Semfri-branded children's multi-purpose helmets are being recalled because they do not comply with the mandatory safety standard for bicycle helmets.
About 8,100 Kitosun Submersible LED Lights are being recalled because they contain lithium coin batteries that children can access easily and lack the warnings required by Reese's Law.
About 500 Andy & Evan children's pajama sets are being recalled because they violate the mandatory flammability standard for children's sleepwear.
About 50 Furnulem five-drawer dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children.
Hyundai is recalling certain 2026 Kona vehicles because the front steering knuckles may crack and break due to a manufacturing error, which can cause loss of steering control and increase crash risk.
Hyundai is recalling certain 2025-2026 IONIQ 5 and 2026 IONIQ 9 vehicles because the high voltage battery system may contain an improperly tightened bus bar, which can cause a short circuit.
About 1,140 Little Cow Co. 9 oz candles in glass jars are being recalled because the jar can crack or break during use.
About 3,500 Cobelae Busy Books for toddlers are being recalled because beads on page eight can loosen and detach, posing a choking hazard.
About 470 bottles of Lotus Joy Organic Sweet Birch Essential Oil are being recalled because the methyl salicylate they contain is not in child-resistant packaging.
About 6,800 YITA 16-drawer dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children.
SunMed Holdings is recalling 95,300 units of the Broselow Pediatric Emergency Rainbow Tape because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.
SunMed Holdings is recalling 89 units of the Filled Broselow Organizer, model 7730IALS, because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.
Superfoods, Inc. is recalling Live it Up brand Super Greens powder, net weight 8.5oz, because the products may be contaminated with Salmonella Typhimurium.
Superfoods, Inc. is recalling 795,834 units of Live it Up brand Super Greens because the products may be contaminated with Salmonella Typhimurium.
SunMed Holdings is recalling 20,583 units of the Broselow Pediatric Emergency Rainbow Tape, model 7700RE, because it contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.
Fontaine Modification is recalling certain 2024-2025 Freightliner Business Class M2 vehicles because the steering gearbox assembly may have been assembled with insufficient oil.
Weaver's Brew is recalling 421 cases of Goldenroot Lemon Ginger Jalapeno Ginger Beer because the products might contain ginger juice that did not undergo the required pasteurization process.
LSL Healthcare is recalling 1,400 Central Line Dressing Kits because the BD ChloraPrep Triple Swabsticks inside exhibit an open seal on the applicator packaging.
Aju Pharm is recalling 233 units of the Fixone Hybrid Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Philips North America is recalling 9 units of the MR 7700 MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Philips North America is recalling 3 units of the SmartPath to dStream for XR and 3.0T because exported MR Elastography stiffness maps may show stiffness value errors.
Siemens is recalling 7 units of the LUMINOS Q.namix T fluoroscopic X-ray system because ortho images may not be flipped as preset and an image of a previous patient may be processed.
Philips North America is recalling 10 units of the Ingenia 1.5T MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Gold Star Distribution is recalling toothbrushes and toothpaste-with-brush packs over potential exposure of rodents and rodent activity in its distribution center.
NIPRO Technical Services is recalling 499 units of Conductivity Standard Solution because a defect in the solution can cause meters to report incorrect conductivity values for dialysate.