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.
Gold Star Distribution is recalling Excedrin over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Boston Scientific is recalling 21 Coyote over-the-wire PTA balloon dilatation catheters over the potential for inflation and deflation difficulty during use in the peripheral vasculature.
Ford is recalling 2025 F-59 and F-53 vehicles because an incorrectly installed switch may cause brake lights to malfunction, increasing crash risk.
Gold Star Distribution is recalling Carmex over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Gold Star Distribution is recalling DayQuil Cold and Flu over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Gold Star Distribution is recalling Pepcid Complete over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Gold Star Distribution is recalling Liquid DayQuil over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
GE HealthCare is recalling 12 units of the SMV BodyTrack nuclear medicine system, because systems moved without adequate detector support may suffer a detector fall.
Philips Medical Systems Nederland is recalling 990 Azurion R3.0 systems over nine identified software issues, including loss of X-ray after a pedal tap and continuous restart.
Gold Star Distribution is recalling Deodorant products over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
ICU Medical is recalling 64,290 Pulsator Arterial Blood Sampling Kits because syringes may have a crack on the collar, which may lead to blood leakage and repeated draws.
WhiteWave is recalling 4,665,608 US units of So Delicious Dairy Free Salted Caramel Cluster Cashewmilk non-dairy frozen dessert over foreign material.
Gold Star Distribution is recalling NyQuil Cold and Flu over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Medline is recalling 33 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Medline is recalling 5314 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Philips Medical Systems Nederland is recalling 8 units of the Allura Xper FD20/20, model 722038, because the drip tray beneath the cooling unit may not have been installed.
Philips Medical Systems Nederland is recalling 18 units of the Allura Xper FD20 Biplane, model 722008, because the drip tray beneath the cooling unit may not have been installed.
Medline is recalling 633 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Philips Medical Systems Nederland is recalling 38 Allura Xper FD10C systems because the drip tray beneath the cooling unit may not have been installed.
Encon Safety Products is recalling 7,677 bags of AQ 120 GFEW Aquarion Preserved Cartridges over cGMP deviations.
Hangzhou Bever Medical Devices is recalling 149,310 BD Ready-to-Use Hydrophilic Catheters, 14 Fr, over a labeling error giving an incorrect expiration date.
Philips Medical Systems Nederland is recalling 22 units of the Allura Xper FD10/10, model 722027, because the drip tray beneath the cooling unit may not have been installed.
Medtronic is recalling 7,123 units of the Vanta Clinician Programmer Application after complaints that it does not function as intended during use.
Heraeus Medical is recalling PALACOS MV pro 40 and PALACOS MV pro 80 bone cement because an unfortunate combination of factors can leave ampoules unbroken, so no appropriate cement dough is formed.
Philips Medical Systems Nederland is recalling 2 Allura Xper FD20 systems because the drip tray beneath the cooling unit may not have been installed.