State
73,584 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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Teva Pharmaceuticals is recalling Epoprostenol Sodium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Teva Pharmaceuticals is recalling Dacarbazine for Injection USP because manufacturing areas exceeded microbial recovery levels, compromising sterility assurance.
Haro Bicycles is recalling approximately 510 Masi Evoluzione and Gran Corsa bicycles from model years 2017-2020 because the fork steerer tube can break, causing riders to lose control and fall.
Ortho-Clinical Diagnostics is recalling deformed VITROS Chemistry VersaTips that may cause assay results to be biased by up to +/-16%.
Northgate Technologies is recalling 25 ConMed 50L abdominal insufflators because an internal tubing component was made with untested material.
Altec is recalling 2017-2019 DC1317 and DRM12 wood chippers because a flexible exhaust pipe section may separate, creating an exhaust gas leak that increases the risk of a fire.
Natus Manufacturing Limited is recalling 7 units of the EDS 3 CSF External Drainage System because the device failed to meet pyrogen test requirements for endotoxins.
Respironics is recalling 94 Philips V60 ventilator batteries because they were shipped without proper design verification. The recall covers distribution across multiple U.S. states.
Litehouse Inc is recalling Brite Harbor Caesar Dressing & Dip because the product contains undeclared anchovies, a potential allergen.
Smiths Medical is recalling specific lots of Bivona Cuffless FlexTend Tracheostomy Tubes because they may have been packaged with the wrong neck flange, posing a risk of patient injury.
Nissan is recalling 2016-2019 Sentra vehicles because a contaminated brake light switch may prevent brake lights from illuminating, increasing crash risk.
Covidien is recalling Parietex hydrophilic anatomical mesh where the package label indicates left-side use but contains a right-side device. This labeling error can lead to implant failure and hernia recurrence.
Volkswagen is recalling certain 2021 Atlas and Atlas Cross Sport vehicles due to improperly machined wheel lug bolt holes that may prevent wheels from attaching properly, risking wheel separation and crashes.
Silk Road Medical is recalling 455 ENROUTE Transcarotid Stent Systems because the tip/nose cone may detach from the device.
Northgate Technologies is recalling 45 Steris CO2MPACT Endoscopic Insufflator systems because an internal tubing component was made with incorrect, untested material.
Ecolab is recalling specific lots of ORS-320 Slush + Warmer Disc Drapes because manufacturing slits may breach the sterile barrier, posing an infection risk to patients.
Baxter Healthcare is recalling 589,704 infusion pumps due to battery performance issues related to prolonged storage.
Dr. Reddy's Laboratories is recalling specific lots of Imatinib Mesylate 100mg tablets because they failed to meet required dissolution specifications.
Areva Pharmaceuticals is recalling 3,287 vials of Irinotecan Hydrochloride Injection due to manufacturing quality deviations identified in a Warning Letter.
Siemens is recalling 41 ARTIS Icono systems with software version VE20B due to misleading error messages and manual gaps that may cause procedure termination.
Medline Industries is recalling specific lots of STAT-Site B-HB controls because the products were compromised during shipment. The recall affects 46 units distributed in Mississippi, Ohio, and Illinois.
Ferrara is recalling 2009-2020 Aerial vehicles because a defective waterway trolley can detach and fall, posing a risk of injury or death.
Forest River is recalling 2021 Coachmen Catalina 184BHS and 184 BHS-W travel trailers because incorrectly installed interior plates may cause the slide-room to partially detach during transit.
Hyundai is recalling 2019-2020 Kona Electric and 2020 Ioniq Electric vehicles because the lithium-ion battery may short-circuit, increasing the risk of a fire.
Milky Way International Trading Corp. is recalling approximately 297,715 pounds of canned corned beef products that were imported and distributed in the U.S. without FSIS import re-inspection.