State
73,190 recalls have nationwide distribution and so reach Oregon. 7,529 additional recalls listed Oregon specifically in their distribution scope.
Of the 7,529 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 1,805 (24%) are Severe.
Which agencies issued them
These figures cover only the 7,529 recalls whose distribution notice names Oregon specifically. The 73,190 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chrysler is recalling 1,240 Mopar steering column control modules that may cause high beams and turn signals to activate incorrectly, increasing crash risk.
Certain 2023-2024 RAM 2500 vehicles and related models have a faulty steering column control module that may cause turn signals and high beams to malfunction, increasing the risk of a crash. Owners should contact FCA US, LLC for free repairs.
Ford is recalling 2022 F-150 vehicles because parking lights may flicker when headlights are on, reducing visibility and increasing crash risk.
KME is recalling 2021-2023 fire trucks because a valve defect may delay parking brake engagement, increasing crash risk.
BMW is recalling specific 2014-2015 X3, X4, and X5 vehicles because the driver's airbag inflator may explode during deployment, posing a risk of serious injury or death.
Micro Bird is recalling certain G5 school buses because wheelchair track anchorages may detach during a crash, increasing injury risk.
A fuel pipe assembly in 2023-2024 McLaren Artura vehicles may detach, causing fuel leaks that increase the risk of engine fires. Dealers will replace the affected assembly free of charge.
Jaguar Land Rover is recalling 121 modified 2023 Defender 130 vehicles because improperly reinstalled brake calipers may detach, reducing braking ability and increasing crash risk.
Chrysler is recalling specific Mopar Hybrid Service Kit Battery Packs because they may fail internally and cause a fire while parked or driving.
A software bug in Philips Brilliance CT scanners causes image-fusion errors, resulting in incorrect radiation therapy coordinates and potential treatment planning failures.
Volvo Trucks is recalling certain 2023-2024 VN trucks because the accelerator pedal position sensor may disconnect, preventing the engine from returning to idle quickly. This can cause loss of vehicle control and increase crash risk.
Microbiologics Inc recalls KWIKSTIK microbiological reagent kits due to Aspergillus flavus contamination in bulk pellets. Affected products were distributed worldwide, including the US, Italy, France, Turkey, Peru, and Mexico.
The IBA Proton Therapy System's patient positioning system can perform unexpected motions, risking patient crushing. Five US units and nine international units are affected.
Medline is recalling 4,850 adult blood culture collection kits (lot numbers 23EMI373, 23EMF712, 23DMF155, 23CMH026) because components inside expired before the kit's labeled expiration date.
Physio-Control is recalling LIFEPAK 15 defibrillators due to a potential defect where battery pins may become loose, causing power issues.
Physio-Control is recalling LIFEPAK 15 defibrillators due to loose battery pins that may cause power failure. Users should verify device functionality immediately.
Physio-Control is recalling LIFEPAK 15 defibrillators due to potential loose battery pins that could cause power failure. Four affected units have been distributed to Arizona, California, North Carolina, New Jersey, and New York.
Physio-Control has recalled LIFEPAK 15 defibrillators because battery pins may become loose, causing power issues. Owners should contact the manufacturer for instructions on how to proceed.
Ricon is recalling Threshold Warning System Kits for wheelchair lifts because the red beacon may not be bright enough, increasing injury risk.
Atrium Medical Corporation is recalling Express Dry Seal Chest Drains (models 4000-100N and 4050-100N) due to inadequate instructions for proper catheter and patient tube connection setup. No injuries have been reported.
Philips Spectral CT on Rails software version 5.1.0 may fail to move the needle position to the desired location during scans. This could cause the gantry to move unexpectedly and potentially collide with the user or needle.
Microbiologics Inc is recalling LYFO-DISK P. venetum laboratory culture disks (lot 794-142) found contaminated with Aspergillus flavus during complaint investigation. The product was distributed worldwide.
Physio-Control is recalling 8 LIFEPAK 15 defibrillators due to loose battery pins that may cause power loss. Affected units were distributed in Arizona, California, North Carolina, New Jersey, and New York.
Mack is recalling 650 2023–2024 trucks due to a sensor defect that can prevent the engine from returning to idle quickly, risking loss of vehicle control. The company will replace the throttle pedal and update software at no cost.
Medline's blood culture kit is being recalled because components inside the kit have expired before the kit's stated expiration date. This could affect the kit's ability to function properly.