The Recall Desk

State

Oregon product recalls

73,486 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.

These figures cover only the 7,533 recalls whose distribution notice names Oregon specifically. The 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24026–24050 of 81019

  • SevereFDA (Food)·F-0462-2022·2022-01-19

    Mind Functions Brainology Capsules Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling Mind Functions Brainology Capsules (132ct bottle) because the product contains undeclared milk, a common allergen.

    Product
    Mind Functions, Inc Brainology Capsules 132ct Bottle UPC CODE 6 31661 48705 5
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0491-2022·2022-01-19

    SRS Nutra LTD Physio Flex Joint Support Capsules Recalled for Undeclared Shellfish

    NutraCap Labs LLC is recalling SRS Nutra LTD Physio Flex Joint Support Capsules due to undeclared shellfish in the product. Consumers with shellfish allergies should not use this product.

    Product
    SRS Nutra LTD Physio Flex Joint Support Capsules 60ct Bottle NO UPC CODE
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0405-2022·2022-01-19

    AIOS Synergy for Men Capsules recalled for undeclared milk

    NutraCap Labs LLC is recalling AIOS Synergy for Men Capsules (120ct bottles) because the product contains undeclared milk. The recall affects lot 2102130 with an expiration date of 02/2023, distributed across 25 states.

    Product
    AIOS Synergy for Men Capsules 120ct Bottle
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0470-2022·2022-01-19

    Nutra Black Recovery Chocolate Recalled for Undeclared Shellfish

    NutraCap Labs LLC is recalling Nutra Black Recovery Chocolate 128oz jars (Lot #2001230, exp. 01/2022) distributed across 25 states because the product contains undeclared shellfish, which poses a risk to consumers with shellfish allergies.

    Product
    Nutra Black Recovery Chocolate 128oz jar NO UPC CODE
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0426-2022·2022-01-19

    DH Nutra Define Thermogenic Capsules Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling DH Nutra Define Thermogenic Capsules because the product contains undeclared milk, a common allergen that poses a risk to consumers with milk allergies.

    Product
    DH Nutra Define Thermogenic Capsules 90ct Bottle UPC CODE
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0495-2022·2022-01-19

    Unlocked Supplements Sana Capsules Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling Unlocked Supplements Sana Capsules (90ct bottles, UPC 6 79360 63826 2, Lot #2004014) because the product contains undeclared milk, a major allergen. The product was distributed across 25 states.

    Product
    Unlocked Supplements Sana Capsules 90ct Bottle UPC CODE 6 79360 63826 2
    Category
    Consumer Product
    Distribution
    26 states
  • SevereFDA (Food)·F-0460-2022·2022-01-19

    Mass Nutraceuticals Brain Food Capsules Recall for Undeclared Milk

    Mass Nutraceuticals Brain Food Capsules are being recalled because they contain undeclared milk. The product was distributed across 25 states and may pose a risk to consumers with milk allergies.

    Product
    Mass Nutraceuticals Brain Food Capsules 120ct Bottle UPC CODE 7 28614 77466 6
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0404-2022·2022-01-19

    Adrenalyne Razzled Up Blue Raspberry Recalled for Undeclared Shellfish

    NutraCap Labs LLC is recalling Adrenalyne Razzled Up Blue Raspberry 25oz jars because the product contains undeclared shellfish, which poses a risk to consumers with shellfish allergies.

    Product
    Adrenalyne Razzled Up Blue Raspberry 25oz jar
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0477-2022·2022-01-19

    Premier Dynamic Nutrition Kinetic Greens Green Lemonade Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling Premier Dynamic Nutrition Kinetic Greens Green Lemonade 25oz jars because they contain undeclared milk, a common allergen. The product was distributed across 25 states.

    Product
    Premier Dynamic Nutrition Kinetic Greens Green Lemonade 25oz Jar UPC CODE
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0415-2022·2022-01-19

    Bic Nutrition Olympus Fruit Punch Recalled for Undeclared Shellfish

    NutraCap Labs LLC is recalling Bic Nutrition Olympus Fruit Punch 64oz bottles due to undeclared shellfish. The product was distributed across 25 states and poses a risk to consumers with shellfish allergies.

    Product
    Bic Nutrition Olympus Fruit Punch 64oz UPC CODE 8 60002 94601 6
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0459-2022·2022-01-19

    Macro Supps ONE Greens Strawberry Kiwi Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling Macro Supps ONE Greens Strawberry Kiwi 25oz jars because the product contains undeclared milk, which poses a hazard to consumers with milk allergies.

    Product
    Macro Supps ONE Greens Strawberry Kiwi 25oz Jar NO UPC CODE
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0441-2022·2022-01-19

    Global Link ShredFX Popsicle Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling Global Link ShredFX Popsicle 16oz jars because the product contains undeclared milk. Consumers with milk allergies or sensitivities are at risk.

    Product
    Global Link ShredFX Popsicle 16oz Jar UPC CODE 9 34585 60024 66
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0417-2022·2022-01-19

    Black Magic Brain Waves Capsules recalled for undeclared milk

    NutraCap Labs LLC is recalling Black Magic Brain Waves Capsules 120ct bottles because the product contains undeclared milk. Consumers with milk allergies or sensitivities are at risk.

    Product
    Black Magic Brain Waves Capsules 120ct Bottle UPC CODE 0 74647 77431 6
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0493-2022·2022-01-19

    TM Nutrition Restoration Pineapple Recalled for Undeclared Milk

    NutraCap Labs LLC is recalling TM Nutrition Restoration Pineapple 19oz jars because the product contains undeclared milk, a common allergen. The recall affects 80,169 units distributed across 25 states.

    Product
    TM Nutrition Restoration Pineapple 19oz Jar UPC CODE 0 746477 745166
    Category
    Food
    Distribution
    26 states
  • HighFDA (Food)·F-0391-2022·2022-01-19

    Classic Lasagna Pasta Sheets Recalled for Undeclared Wheat Allergen

    Local Fixe LLC is recalling Classic Lasagna Pasta sheets because the label declares flour as an ingredient but fails to declare wheat, which is present in the product. Consumers with wheat allergies may face serious health risks.

    Product
    Classic Lasagna Pasta sheets sold frozen and wrapped in brown freezer paper. The weight per package is 1 lb/453.6 grams. The label is read in parts: "***Classic Lasagna sheets *** Ingredients: Flour, Semolina, Egg, water ***www.localfixe.com***".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0476-2022·2022-01-19

    Philips wireless footswitches for Allura Xper and Azurion X-ray systems recalled for connection issues

    Philips wireless footswitches used with Allura Xper and Azurion X-ray systems may experience connection issues that interrupt fluoroscopic imaging during patient procedures. The recall affects 1,971 systems distributed worldwide.

    Product
    Wireless Footswtich used with the following Philips Allura Xper and Azurion Interventional Fluoroscopic X-ray System . Model Number: 722001, 722002, 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722014, 722015, 722019, 722020, 722022, 722023, 722024, 722025…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0491-2022·2022-01-19

    Medtronic Perfusion Kits Recalled: Missing Endotoxin Testing

    Medtronic is recalling approximately 6,653 Custom Perfusion kits used in cardiac procedures because they were labeled as non-pyrogenic without completing required endotoxin testing.

    Product
    Medtronic Custom Perfusion kits, with the following product descriptions and corresponding model numbers: 1. CUSTOM PACK BB10Q85R FILTER (Model BB10Q85R); 2. CUSTOM PACK BB11C01R MIDI DEEP (Model BB11C01R); 3. CUSTOM PACK BB7H95R22 HYP MAIN (Model B7H95R22)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0474-2022·2022-01-19

    Computed Tomography System Software May Degrade Head Image Quality

    Siemens SOMATOM Edge Plus CT systems running software version VB20_SP5 may produce degraded head images, potentially leading to patient misdiagnosis.

    Product
    SOMATOM Edge Plus-Computed tomography system Model 1026700
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0389-2022·2022-01-19

    Pie Dough Recall: Undeclared Wheat Allergen

    Local Fixe LLC is recalling frozen pie dough products because wheat is not declared on the label, even though flour—which contains wheat—is an ingredient. The recall affects 181 packages distributed in Oregon.

    Product
    Pie Dough are packaged two crusts per pack and sold frozen. They are wrapped in white butcher paper. The weight per package is 1.257 lbs/540 grams. The label is read in parts: "***Pie Dough*** Flour, Butter (cream, milk, salt), Organic Palm Shortening, water, salt…
    Category
    Food
    Distribution
    1 state
  • HighCPSC·22054·2022-01-19

    FRIGG Silicone Pacifiers Recalled Due to Choking Hazard

    Mushie & Co is recalling about 333,725 FRIGG Silicone Pacifiers because the silicone nipple can detach from the plastic shield, posing a choking hazard. Eight detachments have been reported in the U.S. with no injuries.

    Product
    FRIGG Silicone Pacifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0477-2022·2022-01-19

    OCT-Camera Laser Shut-Off Malfunction Poses Patient Safety Risk

    Haag-Streit OCT-Camera devices with automatic laser shut-off malfunction may fail to recognize when the laser is safely switched off, posing a potential safety risk.

    Product
    OCT-Camera 211 01 A1, Running software iOCT-Control 3 v1.4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22055·2022-01-19

    Children's Sleepwear Recalled for Flammability Standards Violation

    Childrensalon is recalling about 180 children's sleepwear garments that fail to meet U.S. flammability standards, posing a burn injury risk. Consumers should stop using the garments immediately and contact Childrensalon for return instructions.

    Product
    Children's Sleepwear Garments
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0388-2022·2022-01-19

    Fresh Flour Tortillas Recalled for Undeclared Wheat Allergen

    Local Fixe LLC is recalling Fresh Flour Tortillas because wheat is not declared on the label, even though flour (a wheat product) is listed as an ingredient. This poses a risk to consumers with wheat allergies.

    Product
    Fresh Flour Tortillas are packaged in a clear Ziploc style plastic bag. The weight per package is 1.323 lbs/600 grams. The label is read in parts: "***Fresh Flour Tortillas ***Flour, water, organic palm shortening, salt, baking powder*** ww.localfixe.com***".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0472-2022·2022-01-19

    CT Scanner Software Defect May Degrade Image Quality Nationwide

    Siemens SOMATOM Confidence CT scanners with software version VB20_SP5 may experience degraded head image quality, creating a potential risk of misdiagnosis. The recall affects 108 units distributed nationwide.

    Product
    SOMATOM Confidence -Computed tomography systems Model 10590100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0492-2022·2022-01-19

    Flat Panel Detector May Display Abnormal Images During Surgical Procedures

    Canon Medical's flat panel detectors used in Alphenix surgical systems may display abnormal horizontal stripes and fail to recover by restarting, potentially causing operators to work without proper visual guidance during procedures.

    Product
    Flat Panel Detector, Model Number: TFP-800A, used with the Alphenix Systems, Item Numbers: INFX-8000V, INFX-8000C, INFX-8000F, and INFX-8000H.
    Category
    Medical Device
    Distribution
    Distributed nationwide