The Recall Desk

State

Oregon product recalls

73,381 recalls have nationwide distribution and so reach Oregon. 7,531 additional recalls listed Oregon specifically in their distribution scope.

What the numbers show

Total
7,531
Critical
876
Severe
2,128
Most recent
2026-10-07

Of the 7,531 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 7,531 recalls whose distribution notice names Oregon specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21001–21025 of 80912

  • HighFDA (Food)·F-1452-2022·2022-07-27

    Chocolate Truffles Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling All Milk Classic Truffles (1.4 oz) because they may contain undeclared tree nuts, posing a risk to consumers with tree nut allergies.

    Product
    All Milk Classic Truffle. Net Wt. 1.4 oz. PLU Code: 788394 11275 1. Ingredients: Milk chocolate, honey, butter (pasteurized cream & salt), cream, non-fat dry milk, whey, agar, align & lecithin. Note: Typo on website should be algin.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1413-2022·2022-07-27

    Hill-Rom Mattress Microclimate Feature Failure Increases Pressure Ulcer Risk

    Certain Hill-Rom PRO+ MRS mattresses may have a Microclimate Management feature failure that increases patient pressure ulcer risk. Affected units were distributed to 25+ U.S. states and Canada.

    Product
    Hill-Rom PRO+ MRS Surface For Versacare With X-Ray mattress, REF P3255A01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1491-2022·2022-07-27

    Honeymoon Patties Mint Bee Patties recalled for undeclared tree nuts

    Queen Bee Gardens is recalling Honeymoon Patties Mint Bee Patties because they may contain undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts). The product was sold at retail locations in Colorado, New Mexico, Wyoming, and nationwide online.

    Product
    Honeymoon Patties Mint Bee Patties. Net wt. 8 oz. PLU Code: 788394 14896 5
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1412-2022·2022-07-27

    Hill-Rom PRO+ Mattress Microclimate Management Failure Increases Pressure Ulcer Risk

    Baxter Healthcare is recalling 404 Hill-Rom PRO+ 36" mattresses due to performance degradation in their heat and moisture management feature. This failure increases the risk of pressure ulcer development in patients.

    Product
    Hill-Rom PRO+ 36" MRS Surface mattress, REF P7924A03.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1466-2022·2022-07-27

    QBee Honeycomb Toffee Milk recalled for undeclared tree nuts

    Queen Bee Gardens is recalling QBee Honeycomb Toffee Milk due to undeclared tree nuts. Consumers with tree nut allergies face a potential allergic reaction risk.

    Product
    QBee Honeycomb Toffee Milk. Net wt. 1.5 oz. PLU Code: 788394 10404 6.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1430-2022·2022-07-27

    SIGNA Premier MRI scanner recalled for elevated acoustic noise hazard

    GE Healthcare's SIGNA Premier MRI scanner is being recalled because under rare conditions, the gradient coils can produce elevated acoustic noise that could potentially cause hearing loss with prolonged exposure.

    Product
    SIGNA Premier magnetic resonance scanner, model 5748519.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1480-2022·2022-07-27

    Queen Bee Honey Caramels Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honey Caramels Red Raspberry because the product may contain undeclared tree nuts. The recalled items were distributed to Queen Bee retail stores in Colorado, New Mexico, and Wyoming, and nationwide via internet sales.

    Product
    Honey Caramels Red Raspberry. Net wt. 5.87 oz. PLU Code: 788394 12143 2. Ingredients: Honey, Butter (Pasteurized Cream & Salt), Cream, Freeze dried Raspberries, Grade A Non-Fat Dry Milk, Whey, Natural Flavors, Agar, Algin and Lecithin.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1445-2022·2022-07-27

    Spinal fusion cross connector recalled for insufficient clamping force

    Aesculap is recalling AESCULAP S4 Cervical Cross Connectors used in spinal fusion surgery due to insufficient clamping force that may cause the connectors to loosen or shift on the spinal rods.

    Product
    AESCULAP S4 Cervical Cross Connector, L26mm, S4C CROSS CONNECTOR FIXED 26MM, product code SW114T. Used in spinal fusion surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1437-2022·2022-07-27

    BD Connecta Plus1 360 Infusion Connector: Potential Housing Leakage

    Becton Dickinson is recalling certain BD Connecta Plus1 360 Blue Blend infusion connectors due to potential leakage at the housing stopcock that could interrupt treatment and expose patients to contamination and biohazardous material.

    Product
    BD Connecta" Plus1 360 Blue Blend Catalog No. 394911 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1484-2022·2022-07-27

    Honeymoons Dark Chocolate Almond Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honeymoons Dark Chocolate Almond for undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. The product was distributed to retail locations in Colorado, New Mexico, and Wyoming, and nationwide online.

    Product
    Honeymoons Dark Chocolate Almond. PLU Code: 788394 14792 0.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1272-2022·2022-07-27

    Neostigmine Methylsulfate Injection Recalled for Lack of Sterility Assurance

    Nephron Sterile Compounding Center is recalling 64,365 syringes of Neostigmine Methylsulfate Injection nationwide due to lack of assurance of sterility. Patients using affected lots should contact their healthcare provider.

    Product
    Neostigmine Methylsulfate Injection, USP, 5 mg/5 mL (1 mg/mL) syringe, packaged in 5 x 5 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-902-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1475-2022·2022-07-27

    Honey Caramels Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honey Caramels Cinna Honey due to potential undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts). Affected products were sold at 10 retail locations in Colorado, New Mexico, and Wyoming, as well as nationwide via internet.

    Product
    Honey Caramels Cinna Honey. Net wt. 5.87 oz. PLU Code: 788394 12404 4. Ingredients: Honey, butter (pasteurized cream & salt), cream, nonfat dry milk, whey, cinnamon oil, beet juice (color), lecithin, algin & agar.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1476-2022·2022-07-27

    Honey Caramels Creamy Fudge Recalled for Undeclared Tree Nuts

    Queen Bee Gardens, LLC is recalling Honey Caramels Creamy Fudge because the product may contain undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, and walnuts). People with tree nut allergies should not consume this product.

    Product
    Honey Caramels Creamy Fudge. Net wt. 5.87. PLU Code: 788394 12354 2.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1419-2022·2022-07-27

    Orthopedic Surgical Guide with Defective Spring Subject to Corrosion

    DePuy Orthopaedics is recalling 872 units of the ATTUNE Measured Sizing and Rotation Guide due to a manufacturing defect. A galvanized steel spring was used instead of stainless steel, which may cause corrosion and surgical complications.

    Product
    ATTUNE Measured Sizing and Rotation Guide-to size the femur and align rotation of the bone cuts in preparation for the femoral implant Part Number: 254400525
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1432-2022·2022-07-27

    BD Connecta Stopcock Recalled for Potential Housing Leakage

    Becton Dickinson is recalling its BD Connecta Stopcock due to potential leakage at the housing component, which may interrupt treatment and cause exposure to biohazardous material.

    Product
    BD Connecta Stopcock Without Extension Tube Catalog No. 394600 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1265-2022·2022-07-27

    Morphine Sulfate Injection Recalled for Lack of Sterility Assurance

    Nephron Sterile Compounding Center is recalling Morphine Sulfate Injection due to lack of assurance of sterility. The recall affects 5,495 pre-filled syringes distributed nationwide.

    Product
    Morphine Sulfate Injection, USP, 50 mg/50 mL (1 mg/mL) syringe, packaged in 5 x 50 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-979-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1477-2022·2022-07-27

    Honey Caramels Huckleberry Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honey Caramels Huckleberry (5.87 oz) because they may contain undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. This poses a serious health risk to people with tree nut allergies.

    Product
    Honey Caramels Huckleberry. Net wt. 5.87 oz. PLU Code: 788394 12623 9. Ingredients: Honey, butter (pasteurized cream & salt), cream, nonfat dry milk, natural flavors, purple cabbage (coloring), whey, lecithin, algin & agar.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1339-2022·2022-07-27

    Dietary Supplement Marketed as Unapproved Drug Recalled by FDA

    Launch Sequence Capsules, a dietary supplement sold in 60-count bottles, were recalled because they were marketed without FDA approval as a drug based on label claims.

    Product
    Launch Sequence Capsules, Dietary Supplement, 60- count bottles, ASIN B07TLPWXDS, UPC Code 641378938375.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1492-2022·2022-07-27

    Honeymoon Cinna-Bee Patties recalled due to undeclared tree nuts

    Queen Bee Gardens is recalling Honeymoon Cinna-Bee Patties due to potential undeclared tree nuts: pecans, almonds, coconut, macadamia nuts, and walnuts. Products were distributed in Colorado, New Mexico, Wyoming, and nationwide online.

    Product
    Honeymoon Cinna-Bee Patties. PLU Code: 788394 14892 7
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1483-2022·2022-07-27

    Honeymoons Milk Chocolate Almond Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honeymoons Milk Chocolate Almond candy due to undeclared tree nuts including pecans, almonds, coconut, macadamia, and walnuts. The product was distributed in Colorado, New Mexico, Wyoming, and nationwide online.

    Product
    Honeymoons Milk Chocolate Almond. PLU Code: 788394 14756 2.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1490-2022·2022-07-27

    Honeymoons Ivory Chocolate Pecan Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honeymoons Ivory Chocolate Pecan due to undeclared tree nuts, which may affect consumers with tree nut allergies. The product was sold at retail locations in Colorado, New Mexico, and Wyoming, plus nationwide internet sales.

    Product
    Honeymoons Ivory Chocolate Pecan. PLU Code: 788394 14730 0
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1285-2022·2022-07-27

    Aripiprazole 20mg Tablets Recalled for Failed Dissolution

    Apotex Corp. is recalling 2,010 bottles of Aripiprazole Tablets 20mg nationwide due to failed dissolution specifications. Tablets may not dissolve properly, potentially affecting medication effectiveness.

    Product
    Aripiprazole Tablets, USP 20 mg, packaged in a) 1,000-count bottle (NDC 60505-2676-8, UPC 3 60505 26768 2), b) 30-count bottle (NDC 60505-2676-3, UPC 3 60505 26763 7), Rx only, Manufactured by: Apotex, Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V542000·2022-07-27

    2022 Volkswagen Golf R Sunroof Switch May Close Unexpectedly

    Volkswagen is recalling certain 2022 Golf R and Golf GTI vehicles because the sunroof touch switch may be too sensitive and inadvertently pressed, causing unintended sunroof auto-closure and risking injury.

    Product
    VOLKSWAGEN — VOLKSWAGEN GTI, GOLF R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1499-2022·2022-07-27

    Dark Raspberry Classic Snack Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Dark Raspberry Classic snacks due to undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts) that may be present, posing a risk to consumers with tree nut allergies.

    Product
    Dark Raspberry Classic. Net wt. 1.4 oz. UPC 788394 10003 1.
    Category
    Food
    Distribution
    Distributed nationwide