State
73,104 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 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Honda is recalling certain 2018-2020 Fit and 2019-2022 HR-V vehicles, previously covered by recall 23V-046, because the rearview camera image may not display when the engine is started with a key.
Medline is recalling about 1.5 million Bed Assist Bar adult bed rails because users can become entrapped between the rail and mattress, posing a risk of asphyxiation. Two deaths have been reported.
Toyota is recalling certain 2022-2023 Tundra and Lexus LX600 vehicles with V35A engines because manufacturing debris can contaminate the engine and cause main bearing failure, stalling the vehicle.
Vicinity Motor Corporation is recalling 2017 Vi33 and 2022 Vi35 buses because low-pressure CNG hoses may leak, creating a fire or explosion risk.
Autocar is recalling 2023-2024 Xpeditor and Legend vehicles because an improperly secured axle lock nut may allow the wheel end to separate, increasing crash risk.
Driverge is recalling 2023-2024 Ford T-350 vehicles because the seat recliner mechanism may not engage, increasing injury risk during a crash.
Compare Brands is recalling ADIOS! Super Vinegar All Natural Cleaner due to deceptive labeling that violates federal hazardous-substances rules, posing risks of poisoning and chemical burns.
About 75 padded crib bumpers sold on AliExpress are being recalled because infants can suffocate if they roll or move into a position that obstructs breathing. Padded crib bumpers are banned under federal law.
Black & Decker is recalling about 44,400 CRAFTSMAN V20 Cordless Tillers/Cultivators because misleading assembly instructions can cause consumers to attach the tines upside down, creating a laceration hazard. No injuries have been reported.
Lion Electric is recalling certain 2024-2025 LionC school buses because the parking brake may malfunction and allow the lever to release without pressing the release button.
American Furukawa is recalling certain driver clock springs that may have been contaminated during manufacturing. This defect can cause electrical failure and prevent the driver's air bag from deploying.
Philips Respironics BiPAP A30 Ventilators may experience interruption or loss of therapy during a Ventilator Inoperative alarm, potentially causing severe respiratory compromise or death in vulnerable patients.
BiPAP A40 ventilators may lose therapy delivery during a Ventilator Inoperative alarm, potentially causing respiratory failure or death in vulnerable patients.
Philips BiPAP V30 Auto Ventilators may interrupt or lose therapy during a Ventilator Inoperative alarm, potentially causing hypoventilation, severe oxygen depletion, or respiratory failure.
Sammy's Milk goat formula is recalled for marketing it as safe for infants. The unapproved product does not comply with FDA infant formula manufacturing requirements.
Philips OmniLab Advanced + Ventilators may experience an alarm condition that interrupts or stops therapy delivery. This interruption may lead to inadequate breathing support, low oxygen levels, and potentially fatal respiratory failure.
OptumHealth Care Solutions LLC is recalling 208 units of the Optum Nimbus II Plus ambulatory infusion pump distributed nationwide due to potential battery failure, system errors, and drug leakage.
Sammy's Milk Goat Milk Toddler Formula is recalled because the manufacturer made false claims it was safe for infants as a sole nutrition source. The product lacks FDA premarket approval and does not meet infant formula manufacturing standards.
Merit Medical Systems is recalling 18 units of Prelude Guide Sheath Roadster due to sheaths labeled as .018 dilators potentially containing .038 dilators instead. The mismatch poses a risk if the wrong-sized component is used during medical procedures.
Cadwell Industries is recalling the Cascade IOMAX Cortical Module because an incorrectly installed insulator could cause electrical arcing and potential patient shock.
A Philips Achieva 3.0T for PET MR diagnostic system (Serial 43006) may have a loose mains distribution unit terminal that could overheat and cause smoke or fire.
Philips is recalling MR RT Upgrades Magnetic Resonance diagnostic systems due to a loose terminal connection in the mains distribution unit that could cause smoke or fire. Two units with serial numbers 70980 and 71569 are affected worldwide.
Unreleased software in Scopis ENT surgical navigation systems causes visual guidance to display inaccurately relative to physical reference points, affecting surgical precision. Affects 705 units nationwide.
Philips is recalling 10 MR System 1.5T Marlin MRI devices worldwide due to a fire and smoke hazard. A loose electrical connection in the mains distribution unit may create a hotspot that causes smoke or fire in hospital technical rooms.
MEDLINE non-sterile syringes (Model 91827) are recalled because piston sizes and configurations are outside the FDA clearance range. The manufacturer is recalling 44,800 units distributed in six U.S. states.