State

Oregon product recalls

73,509 recalls have nationwide distribution and so reach Oregon. 7,533 additional recalls listed Oregon specifically in their distribution scope.

What the numbers show

Total: 7,533
Critical: 876
Severe: 2,128
Most recent: 2026-10-14

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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26126–26150 of 81042

HighFDA (Devices)·Z-2047-2021·2021-07-21
Canon Vantage Galan 3T MRI System Recalled for Fire Risk
Canon Medical System is recalling Canon Vantage Galan 3T MRI systems due to a component that does not meet flame retardancy standards, which could result in smoke or fire. The recall affects units distributed nationwide.
Product
Canon Vantage Galan 3T, REF: MRT-3020 - Product Usage: use as a diagnostic imaging modality that produces cross-sectional transaxial, coronal, sagittal, and oblique images that display anatomic structures of the head or body. Additionally, this system is capable of non-contrast…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2044-2021·2021-07-21
Toshiba Vantage MRI System Recalled for Flame Retardancy Defect
Canon Medical's Toshiba Vantage Tiitan 1.5T MRI systems are being recalled due to a component that does not meet flame retardancy standards. The defect could result in smoke or fire. Affected units were distributed nationwide.
Product
Toshiba Vantage Tiitan 1.5T with Standard gradient, Premium Open-Bore MRI System, REF: MRT-1504 - Product Usage: use as a diagnostic imaging modality that produces cross-sectional transaxial, coronal, sagittal, and oblique images that display anatomic structures of the head or…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2077-2021·2021-07-21
Urethral bulking system needles recalled due to sterility assurance failure
Axonics is recalling BULKAMID urethral bulking system needles that may not have been adequately sterilized despite sterile labeling. Unsterilized surgical needles pose infection risk.
Product
BULKAMID, URETHRAL BULKING SYSTEM model # 50050 containing the component: Bulkamid Needle, REF 230651221C, 2 G x 12 am, sterile, CE 0476
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2050-2021·2021-07-21
EcoFit Cementless Acetabular Cup Plugs May Loosen During Hip Surgery
Central hole cover plugs on EcoFit cementless acetabular cups may come loose during surgical implantation, potentially extending operation time or requiring revision surgery. Fifty-one units in Florida and Texas are affected.
Product
EcoFit cup cementless: Model(Catalog Number)/Description: 02200046 /EcoFit cup cementless 46mm dia incl. central hole cover; 02200048 /EcoFit cup cementless 48mm dia incl. central hole cover; 02200050 /EcoFit cup cementless 50mm dia incl. central hole cover; 02200052 /EcoFit…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2078-2021·2021-07-21
Unifine Pentips Plus pen needles distributed with incorrect needle sizes
Owen Mumford USA is recalling Unifine Pentips Plus pen needles because two cases of 4mm needles were mistakenly packaged as 8mm needles, which could result in patients receiving incorrect needle sizes for their insulin pens.
Product
Unifine Pentips Plus, hypodermic needle - Product Usage: Pen needles with built in pen needle remover.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2071-2021·2021-07-21
Arrow Temporary Pacing Catheter Distributed Without FDA 510K Clearance
Arrow International is recalling its Temporary Pacing Catheter/Introducer Kit because it was marketed without required FDA 510K clearance. Approximately 15 units were distributed in multiple U.S. states.
Product
Arrow Temporary Pacing Catheter/Introducer Kit 5Fr. pacing catheter 6 Fr. introducer Product Code: AI-07155-IK - Product Usage: intended for temporary use in electrophysiology studies for intracardiac stimulation and/or ECG recording.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2068-2021·2021-07-21
Arrow Pacing Catheter Kit Recalled for Missing FDA Premarket Clearance
Arrow International is recalling the Pacing Catheter Kit-Bipolar Electrode Catheter (48 units) due to marketing without required FDA premarket clearance (510K). Units were distributed nationwide in FL, ID, IL, NY, OH, and TX.
Product
Arrow Pacing Catheter Kit-Bipolar Electrode Catheter 5 Fr. 110 cm, Product Code: AI-05210 - Product Usage: intended for temporary use in electrophysiology studies for intracardiac stimulation and/or ECG recording.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V554000·2021-07-21
2021 BMW X2 Seat Belt Retractor Defect Increases Injury Risk
BMW is recalling certain 2021 X2 vehicles because the passenger seat belt retractor may deactivate early, failing to comply with federal safety standards. The defective retractor could increase injury risk in a crash.
Product
BMW — BMW, TOYOTA, MINI 540I, SUPRA, COOPER, COOPER S
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0780-2021·2021-07-21
Living Free Nerve & Muscle Herbal Dietary Supplement Soy Allergen Undeclared
Bea Lydeckers Naturals Inc is recalling Living Free Nerve & Muscle Herbal Dietary Supplement because the label declares lecithin but does not specify that it contains soy lecithin, potentially endangering consumers with soy allergies.
Product
Living Free Nerve & Muscle Herbal Dietary Supplement, 100 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Nerve & Muscle Herbal Dietary Supplement***Herbal and Glandular…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2076-2021·2021-07-21
Medtronic LINQ II Insertable Cardiac Monitor Detection Failure Recall
Medtronic is recalling the LINQ II Model LNQ22 Insertable Cardiac Monitor because it may fail to detect dangerous heart rhythms after a restart. The device was distributed worldwide.
Product
Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21167·2021-07-21
Caldwell E-Max Pro BT Earmuffs Recalled for Fire and Burn Hazards
American Outdoor Brands is recalling Caldwell E-Max Pro BT Earmuffs with rechargeable lithium battery packs due to a soldering defect that can cause the unit to overheat, posing fire and burn hazards. No injuries have been reported.
Product
Caldwell E-Max® Pro BT Earmuffs with rechargeable lithium battery packs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2075-2021·2021-07-21
Medical device software c4D fails to change site upon synchronization
C-RAD POSITIONING AB is recalling Catalyst positioning software c4D because it fails to properly update the Site field during synchronization in the setup workflow. This software defect may prevent correct system configuration.
Product
PC Application Software c4D as part of the device Catalyst: SP-002 Software PA-003 version 6.1.1 and 6.1.0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2045-2021·2021-07-21
Canon 1.5T MRI System Recalled for Flame Retardancy Component Failure
Canon Vantage Tiitan 1.5T MRI Systems with certain serial numbers are recalled due to a component lacking proper flame retardancy, which could result in smoke or fire.
Product
Canon Vantage Tiitan 1.5T, Premium Open-Bore MRI System, REF: MRT-1510 - Product Usage: use as a diagnostic imaging modality that produces cross-sectional transaxial, coronal, sagittal, and oblique images that display anatomic structures of the head or body. Additionally, this…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V555000·2021-07-21
2021 Nissan Rogue Sport Seat Belt Retractor Safety Defect Recall
Nissan is recalling 2021 Rogue Sport vehicles because seat belt automatic locking retractors may deactivate prematurely, reducing protection for child safety seats and violating federal crash protection standards.
Product
NISSAN — NISSAN redundant ROGUE SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2079-2021·2021-07-21
Catheter Sheath Introducer Recalled for Size Labeling Discrepancy
Cordis Corporation is recalling 680 Avanti® Catheter Sheath Introducer units because the actual product dimensions are larger than the labeling indicates.
Product
Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for use in arterial and venous procedures requiring percutaneous introduction of intravascular devices.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0776-2021·2021-07-21
Living Free Adult Extra Multi-Vitamin Recall for Undeclared Soy
Bea Lydeckers Naturals Inc is recalling Living Free "Adult Extra" multi-vitamin capsules because the label declares lecithin but does not declare that it is soy lecithin, posing a risk to consumers with soy allergies.
Product
Living Free "Adult Extra" multi-vitamin, 100 or 500 capsules per bottle. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "**Living Free Adult Extra***Natural Vitamin Mineral Herbal Glandular Supplements***Formulated and…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0777-2021·2021-07-21
Living Free Heart/Blood Vessel Dietary Supplement Recalls for Undeclared Soy
Bea Lydeckers Naturals Inc is recalling Living Free Heart/Blood Vessel Dietary Supplement because the label declares lecithin but does not declare that it is soy lecithin, posing a risk to consumers with soy allergies.
Product
Living Free Heart/Blood Vessel Dietary Supplement, 100 or 500 capsules per bottle. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Heart/Blood Vessel Dietary Supplement***Glandular Herbal & Vitamin…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0778-2021·2021-07-21
Living Free Immune Dietary Supplement Soy Allergen Mislabeling Recall
Bea Lydeckers Naturals Inc is recalling Living Free Immune Dietary Supplement because the label declares lecithin but does not declare that it contains soy lecithin, posing a risk to consumers with soy allergies.
Product
Living Free Immune Dietary Supplement, 100 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Immune Dietary Supplement***Glandular and Herbal Supplement***Formulated by Beatrice…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2070-2021·2021-07-21
Arrow Bipolar Balloon Electrode Catheter Recalled for Marketing Without FDA 510K Clearance
Arrow International is recalling 4 units of an electrode catheter marketed without FDA 510(k) clearance. The device was intended for electrophysiology studies.
Product
Arrow Bipolar Balloon Electrode Catheter 5 Fr. 105 cm, Product Code: AI-07154 - Product Usage: intended for temporary use in electrophysiology studies for intracardiac stimulation and/or ECG recording.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2046-2021·2021-07-21
Canon MRI System Recalled for Flame-Retardancy Component Defect
Canon Medical System recalled its Vantage Titan 3T MRI systems due to a component lacking proper flame-retardancy standards. The defect could produce smoke or fire during use.
Product
Canon Vantage Titan 3T, Premium Open-Bore MRI System, REF: MRT-3010 - Product Usage: use as a diagnostic imaging modality that produces cross-sectional transaxial, coronal, sagittal, and oblique images that display anatomic structures of the head or body. Additionally, this…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V552000·2021-07-21
Kalmar Recalls 2021 Ottawa T2 Vehicles Due to Stability Control Defect
Kalmar is recalling 2021 Ottawa T2 vehicles because an incorrectly installed rear stability control harness may cause the system to be inactive, increasing crash risk.
Product
KALMAR — KALMAR OTTAWA T2
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0779-2021·2021-07-21
Living Free Lung & Joint Congestion Herbal Dietary Supplement Soy Allergen
Bea Lydeckers Naturals Inc is recalling Living Free Lung & Joint Congestion Herbal Dietary Supplement because the label declares lecithin but does not identify it as soy lecithin, creating an undeclared soy allergen hazard.
Product
Living Free Lung & Joint Congestion Herbal Dietary Supplement, 100 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Lung & Joint Congestion Herbal Dietary Supplement***Glandular…
Category
Food
Distribution
Distributed nationwide
HighNHTSA·21V550000·2021-07-21
2020-2021 Bentley Continental GT Front Seat May Trap Rear Passenger Legs
Bentley is recalling certain 2020-2021 Continental GT vehicles because the front seat may trap a rear passenger's legs during automated movements. The front seat software will be updated free of charge.
Product
BENTLEY — BENTLEY CONTINENTAL GT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0781-2021·2021-07-21
Living Free Nerve & Muscle Plus Supplement Recalled for Undeclared Soy
Bea Lydeckers Naturals Inc is recalling Living Free Nerve & Muscle Plus Cetyl-Myristoleate supplement because the label declares lecithin but does not declare that the lecithin is soy-derived, posing a risk to consumers with soy allergies.
Product
Living Free Nerve & Muscle Plus Cetyl-Myristoleate Herbal and Glandular Supplement, 180 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Nerve & Muscle Plus Cetyl-Myristoleate…
Category
Food
Distribution
Distributed nationwide
ModerateCPSC·21169·2021-07-21
Rite Aid Recalls Rechargeable Handheld Fans Due to Fire Hazard
Rite Aid is recalling about 9,780 rechargeable handheld fans sold nationwide from April through June 2021 because the lithium ion battery can overheat while charging and pose a fire hazard. The company has received two reports of the fans overheating and emitting smoke, though no injuries have been reported.
Product
Rechargeable handheld fans
Category
Consumer Product
Distribution
Distributed nationwide