The Recall Desk

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.

25951–25975 of 81042

  • SevereCPSC·21175·2021-08-04

    LG Energy Solution Recalls RESU10H Home Batteries for Fire Hazard

    LG Energy Solution Michigan is recalling about 10,000 RESU10H lithium-ion residential energy storage batteries because they can overheat and catch fire, emitting harmful smoke. The firm has received five reports of batteries smoking and catching fire, resulting in property damage and one injury.

    Product
    LG Chem "RESU10H" Lithium-Ion Residential Energy Storage System Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0806-2021·2021-08-04

    Eat Gangster Oatmeal Cookie Mix Recalled for Salmonella Contamination

    Eat Gangster Oatmeal Schmoatmeal Cookie Mix has been recalled due to potential Salmonella contamination in tigernut flour, an ingredient used in the product. The affected 8.5 oz bags were distributed nationwide.

    Product
    Eat GANGSTER, Oatmeal Schmoatmeal Cookie Mix, 8.5 Oz, Eat GANGSTER LLC, Wichita, KS, UPC 0 51497 13952 0
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2005-2021·2021-08-04

    Recirculator 8.0s Disposable Lavage Kit recalled for potential aluminum ion release

    Eight Medical International BV is recalling the Recirculator 8.0s Disposable Lavage Kit due to potential aluminum ion release during warming therapy that may expose patients under certain use conditions.

    Product
    Recirculator 8.0s Disposable Lavage Kit (product code number 8100) , GTIN: 08719992086016. Hyperthermic Perfusion System intended to raise the temperature of the thoracic or peritoneal cavity to a target temperature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2161-2021·2021-08-04

    OEC Elite Mobile C-Arm Recalled for Battery Depletion

    GE OEC Medical Systems is recalling 3,570 OEC Elite mobile C-arm imaging systems worldwide due to potential early depletion of the battery that monitors X-ray tube temperature, which could render the system inoperable.

    Product
    OEC Elite mobile C-arm - Product Usage: intended to provide fluoroscopic and digital spot images of the patient anatomy, interventional tools/devices, and contrast agents during diagnostic, interventional, and surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2151-2021·2021-08-04

    CooperVision Contact Lenses Recalled for Misaligned Axis Mark

    CooperVision is recalling MEDIFLEX ELITE 1 DAY TORIC daily disposable contact lenses (lot W0106167) due to misaligned axis marks that can cause blurred vision.

    Product
    MEDIFLEX ELITE 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V608000·2021-08-04

    2021 Porsche Taycan Seat Belt Retractor Defect May Prevent Child Restraint Securing

    Porsche is recalling certain 2021 Taycan models because the seat belt automatic locking retractors may deactivate early, preventing child restraint systems from securing properly during a crash.

    Product
    PORSCHE — PORSCHE 911, PANAMERA 4S, PANAMERA 4 E-HYBRID, PANAMERA TURBO S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21174·2021-08-04

    Two Million Dehumidifiers Recalled for Fire and Burn Hazards

    About 2 million dehumidifiers manufactured by New Widetech under multiple brand names are recalled because they can overheat and catch fire, posing fire and burn hazards. Consumers should stop using them immediately.

    Product
    Dehumidifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2150-2021·2021-08-04

    Contact lens recall: misaligned axis mark may cause blurred vision

    CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot W0106167) due to misaligned axis marks that may cause blurred vision. The recall affects 450 lenses distributed across select U.S. states and multiple countries.

    Product
    CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2149-2021·2021-08-04

    CLARITI 1 DAY TORIC Contact Lenses Recalled Due to Axis Mark Misalignment

    CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot W0106167) due to misaligned axis marks that can cause blurred vision. Affected patients should discontinue use and contact their eye care provider.

    Product
    CLARITI 1 DAY TORIC -DIAGNOSTIC Power-07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2144-2021·2021-08-04

    Contact Lens Axis Mark Misalignment May Cause Blurred Vision

    CooperVision's AQUATECH PLUS 1 DAY TORIC contact lenses (lot R0121629) have misaligned axis marks that may cause blurred vision in patients.

    Product
    AQUATECH PLUS 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2163-2021·2021-08-04

    Coaxial Interventional Needles recalled for potential sterilization failure

    Coaxial Interventional Needles from INNOVATIVE TOMOGRAPHY PRODUCT GMBH may not be properly sterilized. Multiple lot numbers are affected and should not be used.

    Product
    Coaxial Interventional Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. KIR 23/05, Length 50 mm, Diameter 23 G (0.6 mm); Article no. KIR 23/05N, Length 50 mm, Diameter 23 G (0.6 mm); Article no. KIR 23/07, Length 75 mm, Diameter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21E071000·2021-08-04

    Enerco Propane Regulators Recalled Due to Fire Risk

    Enerco Group is recalling specific propane regulators that may fail, causing excessive gas pressure and increased fire risk.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2146-2021·2021-08-04

    CooperVision CLARITI 1 DAY TORIC contact lenses recalled for axis mark misalignment

    CooperVision is recalling CLARITI 1 DAY TORIC daily disposable contact lenses due to misaligned axis marks that can cause blurred vision. Affected lenses in lot U0108833 were distributed in seven US states and internationally.

    Product
    CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V609000·2021-08-04

    Peterbilt 220 Recall for Stator Assembly Wire Crimping Defect

    PACCAR is recalling 2020 Peterbilt 220 trucks with Meritor 14Xe ePowertrains due to insufficiently crimped stator wires that may cause overheating and loss of drive power.

    Product
    PETERBILT — PETERBILT 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2166-2021·2021-08-04

    Medical inflation device recalled due to handle separation risk

    Merit Medical Systems is recalling basixALPHA Inflation Devices due to a design flaw where the syringe handle can separate when withdrawn, affecting device functionality.

    Product
    basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Used to inflate and deflate an angioplasty balloon or other interventional device, and to measure the pressure within the balloon.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V604000·2021-08-04

    Newmar Motorhomes Recalled for Potential Fuel Leak and Fire Risk

    Newmar Corporation is recalling certain 2021-2022 motorhomes (New Aire, Ventana, and Dutch Star) with Cummins L9 diesel engines due to potential fuel leaks that could increase fire risk. Affected owners should contact Newmar customer service at 1-800-731-8300 for free fuel hose replacement.

    Product
    NEWMAR — NEWMAR DUTCH STAR, NEW AIRE, VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2164-2021·2021-08-04

    Semi-automatic Biopsy Needles Recalled Due to Sterilization Defect

    INNOVATIVE TOMOGRAPHY PRODUCT GMBH is recalling semi-automatic biopsy needles because labeled sterile units may not have been adequately sterilized. Affected devices distributed in California should not be used.

    Product
    Semi-automatic Biopsy-Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. BIM 18/10, Length 100 mm, Diameter 18 G (1.25 mm); Article no. BIM 18/15, Length 150 mm, Diameter 18 G (1.25 mm); Article no. BIM 18/20, Length 200 mm…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V603000·2021-08-04

    Lamborghini Recalls 2021 Urus for Rear Seat Belt Retract Defect

    Lamborghini is recalling 2021 Urus vehicles because middle-rear seat belt retractors may deactivate early, preventing child restraints from securing properly.

    Product
    LAMBORGHINI — LAMBORGHINI URUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2160-2021·2021-08-04

    OEC 3D Imaging X-Ray Systems Recalled for Coin Cell Battery Depletion

    GE OEC Medical Systems is recalling certain OEC 3D Imaging fluoroscopic X-ray systems due to potential premature depletion of the coin cell battery used to monitor X-ray tube temperature, which could cause the system to become inoperable.

    Product
    OEC 3D Imaging, Image-Intensified Fluoroscopic X-Ray System, Mobile - Product Usage: designed to provide fluoroscopic and digital spot images of adult and pediatric populations during diagnostic, interventional, and surgical procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2156-2021·2021-08-04

    Affinity Four Birthing Bed Latch Mechanism Defect Poses Fall Risk

    The latch mechanism on the Lift-Off foot section of certain Affinity Four Birthing Beds may be damaged, potentially causing improper engagement and creating a fall risk for patients. Hill-Rom is recalling approximately 1,096 affected beds.

    Product
    Affinity Four Birthing Bed-used as a birthing bed for women of child bearing age in an LDR (Labor, Delivery, Recovery) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market Model Numbers: P3700B, P3700C, P3700D, & P3700E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2162-2021·2021-08-04

    Coaxial Interventional Needles Recalled for Potential Sterilization Defects

    INNOVATIVE TOMOGRAPHY PRODUCT GMBH is recalling Coaxial Interventional Needles distributed in California due to potential sterilization defects. Needles labeled as sterile may not have been adequately sterilized, creating infection risks.

    Product
    Coaxial Interventional Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. KIM 22/05, Length 50 mm, diameter 22G/0,7 mm; Article no. KIM 22/07,Length 75 mm, diameter 22 G (0.7 mm); Article no. KIM 22/10, Length 100 mm, diameter 22 G…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V607000·2021-08-04

    2021 Volkswagen ID.4 rear seat belt assemblies may not secure child restraints

    Certain 2021 Volkswagen ID.4 vehicles have rear seat belt assemblies without proper automatic locking function, preventing child restraint systems from securing correctly. Dealers will inspect and replace affected assemblies at no cost.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2154-2021·2021-08-04

    Daily Toric Contact Lenses Recalled for Misaligned Axis Mark

    CooperVision is recalling SOFMED BREATHABLES 1 DAY TORIC contact lenses (Lot W0106167) due to misaligned axis marks that can cause blurred vision. Affected lenses were distributed in the US and internationally.

    Product
    SOFMED BREATHABLES 1 DAY TORIC Power-07.00 -1.75/ 170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2148-2021·2021-08-04

    Contact Lens Recall: Misaligned Axis Mark May Cause Blurred Vision

    CooperVision is recalling SPECSAVERS UMERE TORIC daily disposable contact lenses with UV blocker due to a manufacturing defect in which misaligned axis marks may cause blurred vision.

    Product
    SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide