State
73,486 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 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
GE Healthcare is recalling the Vscan Extend portable ultrasound device due to battery power failure. The device may not power on when the battery is depleted, particularly if not turned off before battery removal or when connected to a computer without AC power.
Edge Pharma, LLC is recalling 2,204 vials of Cantharidin PLUS, a topical gel-forming suspension used to treat skin conditions. The recall is due to manufacturing quality control deviations discovered during production.
Edge Pharma is voluntarily recalling 353 jars of Profound Dental Gel nationwide due to Current Good Manufacturing Practice (CGMP) deviations identified during the manufacturing process.
Mylan Pharmaceuticals Inc is voluntarily recalling Proctofoam HC (hydrocortisone acetate 1% and pramoxine hydrochloride 1%) topical aerosol due to current Good Manufacturing Practice (cGMP) deficiencies. The recall affects 233,199 10-gram aerosol containers distributed nationwide.
Edge Pharma is recalling Mitomycin-C sterile ophthalmic solution syringes because the manufacturer lacks assurance of sterility. The recall affects 154 syringes distributed nationwide.
Dental Alliance Holdings LLC is recalling the CTx36 Kit because it contains less sodium fluoride than stated on the product label. Affected patients should contact their dentist.
Edge Pharma, LLC is recalling 74 jars of LT Topical Cream (Lidocaine/Tetracaine) nationwide due to deviations from Current Good Manufacturing Practice (CGMP). The firm initiated the voluntary recall on December 6, 2021.
Edge Pharma, LLC is recalling Profound-PE Dental Gel nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The recall affects 175 jars of the topical oral anesthetic gel.
GE Vscan Extend portable ultrasound devices may not power on due to battery depletion caused by improper device handling. The device must be properly turned off before removing the battery or disconnecting from power sources.
CariFree sample boxes containing CTx4 Gel 5000 are being recalled because the product contains less Sodium Fluoride than stated on the label. Affected lots are 492106 and 492107, distributed nationwide.
Ascend Laboratories is recalling Metoprolol Succinate Extended-Release Tablets 25 mg nationwide because the tablets failed to meet dissolution specifications, which may affect how the medication releases in the body.
CariFree CTx4 GEL 5000 (Lot 142017) contains less sodium fluoride than stated on the label. The product is being recalled and consumers should contact their healthcare provider with questions.
Seagrave is recalling 2021 Capitol and Marauder vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake unexpectedly and increasing crash risk.
Jayco is recalling 2021-2022 Pinnacle and North Point trailers with Sailun tires that may experience belt separation, potentially causing loss of vehicle control. Free tire replacement is available through dealers.
Tesla is recalling vehicles with seatbelt warning chimes that may not activate when the driver has not fastened their seat belt. The fix is a free over-the-air software update.
Bridgestone is recalling specific Firestone Transforce tires because an incorrect inner liner compound could cause belt separation, increasing the risk of a crash.
Newmar is recalling 2020-2022 Super Star and Supreme Aire motor homes because a tire valve stem extension may be damaged, causing loss of tire pressure and increasing crash risk.
Samsung SDI is recalling specific high voltage battery packs that may fail, causing a sudden loss of drive power and increasing crash risk.
Mercedes-Benz is recalling 2021 AMG GT Black Series vehicles because an incorrectly sized front wheel speed sensor wiring harness may damage, impairing safety systems and increasing crash risk.
Porsche is recalling 2021-2022 Cayenne vehicles due to potential rear axle misalignment following prior repairs. The defect may cause premature tire wear and increase crash risk.
Forest River is recalling certain 2022 Vengeance Fifth Wheel trailers because the tire pressure labels may display incorrect information for the front tires, which could result in under-inflated tires and increase the risk of a crash.
Grand Design RVs (2013-2021) are recalled for an improperly secured 110-volt refrigerator wire that may cause electrical arcing and fire. Dealers will inspect and replace damaged wiring at no cost.
Johnson Health Tech is recalling about 19,900 Matrix T1 and T3 Series commercial treadmills because the power cord can become loose from the power socket, causing sparking, smoking, melting, and fire. No injuries have been reported.
Grand Design is recalling 2020-2021 Imagine travel trailers with cast aluminum cabinet handles that may have sharp edges. The sharp edges could cut or scrape occupants, and dealers will replace the handles free of charge.
Prevost is recalling certain seat brackets that may not meet strength requirements, increasing injury risk in a crash.