State
72,919 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 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
E Mishan & Sons is recalling Granitestone Diamond Pro Blue sauté pans because the metal cap on the handle screw can detach and forcefully eject when heated. One injury has been reported.
Sleepy Customs LLC is recalling IS300 Slave Cylinder Conversion Kits because the adapter plate may separate, causing loss of clutch function and increasing crash risk.
Graco is recalling specific SnugRide Turn & Slide infant seats because the carrier may detach from the base in a crash, increasing injury risk.
Huizhou Haitan Technology is recalling T400 battery chargers because they can ignite or cause a connected battery to ignite. Thirty-three fires and explosions have been reported.
TecFlox hair and beard growth serum bottles are being recalled because they are not child-resistant, as required for minoxidil under the Poison Prevention Packaging Act.
General Motors is recalling 32,988 Chevrolet Corvette vehicles because a software error may prevent detection of a rear turn signal light failure.
General Motors is recalling 276,879 Chevrolet Malibu vehicles because the rearview camera screen may display a distorted or blank image.
Coluans Christmas Light-Up Rings party favors are being recalled because the battery compartment contains button cell batteries that can be easily accessed by children.
Sangohe adult portable bed rails models 504E and 504Q are being recalled because users can become entrapped within the rail or between the rail and the mattress.
ELENKER-branded adult portable bed rails in three sizes are being recalled because users can become entrapped within the rail or between the rail and the mattress.
OCUN NA is recalling Ocun Condor HMS Triple Locking Carabiners because the gate can malfunction and fail to close automatically, having to be closed by hand.
Beestech spiral children's tower toys are being recalled because they contain small balls and are intended for children under three, violating the mandatory standard for toys.
Keystone RV is recalling 172 Montana fifth wheel recreational trailers because the underbelly may be improperly secured and can detach.
Gavoyeat Halloween Light-Up Rings party favors are being recalled because the battery compartment contains button cell batteries that can be easily accessed by children.
BMW of North America is recalling 9,160 K 1600 motorcycles because a deteriorating seal can let moisture into the reverse gear control unit, causing it to overheat.
Member's Mark Valentine children's pajama sets are being recalled because they violate the mandatory standards for flammability of children's sleepwear.
Tuymec Minoxidil Hair Growth Kits are being recalled because the packaging is not child-resistant, as required for minoxidil under the Poison Prevention Packaging Act.
Philips Respironics is recalling the Trilogy Evo ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Philips Respironics is recalling the Trilogy Evo O2 ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Lucerne 2% Cottage Cheese 24 oz. tubs are being recalled due to the potential presence of metal spring fragments. Consumers who have purchased affected product should not consume it.
Merit Medical is recalling CentrosFLO Hemodialysis Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.
Erbe USA is recalling the Flexible Cryoprobe REF 20402-411 because the probes may rupture or burst during activation. The FDA has classified this recall as Class I.
Philips Respironics is recalling the Trilogy EV300 ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Merit Medical is recalling DuraMax Chronic Hemodialysis Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.
Ajinomoto Foods North America is recalling Teppanyaki Style Vegetable Fried Rice due to the presence of glass fragments ranging from 1–3 cm long. Consumers should not eat affected products and should discard or return them.