The Recall Desk

State

Oregon product recalls

72,940 recalls have nationwide distribution and so reach Oregon. 7,525 additional recalls listed Oregon specifically in their distribution scope.

What the numbers show

Total
7,525
Critical
876
Severe
1,803
Most recent
2026-09-09

Of the 7,525 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 1,803 (24%) are Severe.

These figures cover only the 7,525 recalls whose distribution notice names Oregon specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5326–5350 of 80465

  • SevereCPSC·25475·2025-09-25

    Countertop ovens recalled after 95 reports of doors closing and burning users

    About 1,290,000 Oster French Door Countertop Ovens are recalled because the doors can unexpectedly close. Sunbeam has 95 reports of doors closing and causing burns, including two second-degree burns.

    Product
    Oster French Door Countertop Ovens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25476·2025-09-25

    Cooling gel seat pads recalled after a child suffered second degree burns

    About 20,000 Hoovy Cooling Gel Insert Pads for car seats and strollers are recalled because they can become hot in the sun or a hot car. One child suffered second degree burns requiring medical attention.

    Product
    Hoovy Cooling Gel Insert Pads for Car Seats and Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V643000·2025-09-25

    BMW Recalls 2026 M4 and 430i Vehicles for Fire Risk

    BMW is recalling 2026 M4 and 430i vehicles because improperly connected battery cables may cause engine stalls or fires.

    Product
    BMW — BMW 430I, M4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V651000·2025-09-25

    Altec Recalls 2024-2025 A-Class Vehicles Due to Loose Platform Bolts

    Altec is recalling 2024-2025 A-Class vehicles because platform retaining plate bolts may not have been properly tightened, posing a risk of detachment and injury.

    Product
    ALTEC — ALTEC A-CLASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V648000·2025-09-25

    Bentley high pressure fuel pump joint may be improperly tightened

    Bentley is recalling certain 2025-2026 Continental GT, Continental GTC and 2025 Flying Spur vehicles because the bolted joint securing the high-pressure fuel pump to the V8 engine may be improperly tightened.

    Product
    BENTLEY — BENTLEY CONTINENTAL GT, FLYING SPUR, CONTINENTAL GT CABRIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25477·2025-09-25

    Numbing cream recalled because lidocaine packaging is not child resistant

    About 28,000 RELIEVE numbing cream containers are recalled because the lidocaine product is not in child-resistant packaging as required by the Poison Prevention Packaging Act. No incidents reported.

    Product
    RELIEVE Numbing Cream
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V650000·2025-09-25

    Altec Recalls Aerial Devices Due to Outrigger Pad Fire Risk

    Altec is recalling 2021-2025 aerial devices because the outrigger pad holder may be installed too close to the exhaust, increasing fire risk.

    Product
    ALTEC — ALTEC AN SERIES AERIAL DEVICE, AA SERIES AERIAL DEVICE, AM SERIES AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25C010000·2025-09-25

    Evenflo Recalls Revolve360 Slim Child Seats Due to Foam Choking Hazard

    Evenflo is recalling Gold Revolve360 Slim and Revolve360 Slim child seats because loose headrest foam can break off and pose a choking hazard to children.

    Product
    CHILD SEAT:SHELL:HEADREST recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V649000·2025-09-25

    Kia Sorento blower motor wiring harness may be inadequate causing fire

    Kia is recalling certain 2021-2023 Sorento vehicles because the heating, ventilation and air conditioning blower motor wiring harness may be inadequate, which can result in a fire.

    Product
    KIA — KIA SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V639000·2025-09-25

    Chevrolet Equinox EV pedestrian alert sound may be insufficient

    General Motors is recalling certain 2024 Chevrolet Equinox EV vehicles because the pedestrian alert sound system may not change volume enough between standstill and low speed, failing FMVSS 141.

    Product
    CHEVROLET — CHEVROLET EQUINOX EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V641000·2025-09-25

    International Recalls 2026 IC Bus CECB for Wiper Crank Shaft Defect

    International is recalling 2026 IC Bus CECB commercial buses because a weld on the wiper crank shaft may fail, causing the left-side wiper to stop working.

    Product
    IC BUS — IC BUS CECB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V645000·2025-09-25

    Range Rover Evoque rearview camera can admit water distorting the image

    Land Rover is recalling certain 2023 Range Rover Evoque vehicles because water may enter the rearview camera, so the image may not appear on the display or may appear distorted.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2483-2025·2025-09-24

    Blood and fluid warming sets recalled to clarify flow rates and temperatures

    3M Ranger Blood/Fluid Warming High Flow Sets are the subject of a field action to clarify flow rates, inlet fluid temperatures and the location of the outlet temperature. The FDA classified it as Class I.

    Product
    3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2539-2025·2025-09-24

    SmartDrive MX2-3DCK dials recalled over faulty connection to wheelchair motor

    SmartDrive MX2+ SpeedControl Dials, REF MX2-3DCK, are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. 15,834 units are affected.

    Product
    Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.
    Category
    Medical Device
    Distribution
    52 states
  • CriticalFDA (Drugs)·D-0655-2025·2025-09-24

    Cyclobenzaprine bottles recalled after being filled with meloxicam tablets instead

    Unichem Cyclobenzaprine Hydrochloride Tablets, 10 mg, lot GMML24026A, are recalled because bottles labeled as cyclobenzaprine contained yellow Meloxicam 7.5 mg tablets. The FDA classified the action as Class I.

    Product
    CYCLOBENZAPRINE HYDROCHLORIDE — CYCLOBENZAPRINE HYDROCHLORIDE (CYCLOBENZAPRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2538-2025·2025-09-24

    Wheelchair power assist speed dials recalled over potential loss of control

    SmartDrive MX2+ SpeedControl Dials are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. The FDA classified the action as Class I. 25,389 units are affected.

    Product
    Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.
    Category
    Medical Device
    Distribution
    52 states
  • CriticalFDA (Devices)·Z-2540-2025·2025-09-24

    SmartDrive speed control dials recalled over faulty motor electrical connection

    SmartDrive MX2+ SpeedControl Dials, REF MX2-3DCMC, are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. 8,413 units are affected.

    Product
    Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCMC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.
    Category
    Medical Device
    Distribution
    52 states
  • SevereNHTSA·25V638000·2025-09-24

    Volkswagen and Audi front seat belt retractor torsion bars may be damaged

    Volkswagen is recalling certain 2025-2026 GTI, Golf R, Audi A5, S5, A6 and Q4 e-Tron models because the torsion bar in one or both front seat belt retractors may have been damaged during production.

    Product
    AUDI — AUDI, VOLKSWAGEN Q4 E-TRON, A6 SPORTBACK E-TRON, S5, S6 SPORTBACK E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V637000·2025-09-24

    Audi SQ7 high pressure fuel pump fasteners may be loose

    Volkswagen is recalling one Audi SQ7 vehicle because the fasteners securing the high pressure fuel pump may not be tightened properly, resulting in a fuel leak. The vehicle has been repaired.

    Product
    AUDI — AUDI SQ7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0584-2025·2025-09-24

    Kroger cooked shrimp pieces recalled over possible cesium-137 contamination

    Frozen Mercado Kroger Cooked Shrimp pieces, medium peeled tail-off, in 2 lb packages, are recalled because the product may be contaminated with Cesium-137. 18,000 bags are affected.

    Product
    Frozen Mercado Kroger Cooked Shrimp - Medium - Peeled - Tail-Off - Shrimp Pieces. 2 lbs. package. Net wt. per case 10lbs. (5x2lb packages per case). UPC 011110626196.
    Category
    Food
    Distribution
    30 states
  • HighFDA (Devices)·Z-2573-2025·2025-09-24

    Hematology analyzers recalled over erroneously high hemoglobin results in some samples

    UniCel DxH 690T Coulter Cellular Analysis Systems configured with the LED HGB photometer are recalled because they may produce erroneously high hemoglobin results on samples with elevated white blood cell counts.

    Product
    UniCel DxH 690T COULTER Cellular Analysis System, configured with the Led HGB Photometer REF: C34520
    Category
    Medical Device
    Distribution
    Distributed nationwide