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.

21051–21075 of 80912

  • HighFDA (Drugs)·D-1268-2022·2022-07-27

    Morphine Sulfate Injection Recalled Due to Sterility Assurance Concerns

    Nephron Sterile Compounding Center LLC is recalling morphine sulfate injection syringes due to lack of assurance of sterility. The recall affects 4,620 pre-filled syringes distributed nationwide.

    Product
    Morphine Sulfate Injection, USP, 1 mg/mL syringe, packaged in 5 x 1 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: 69374-979-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1403-2022·2022-07-27

    Radiation treatment planning software fails to propagate treatment course data

    RayStation 9B SP1 radiation treatment planning software has an issue where treatment course information may not be propagated to other systems in some workflows. This could potentially affect treatment planning accuracy.

    Product
    RayStation 9B SP1. For radiation treatment planning.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1496-2022·2022-07-27

    Truffle Dark Gift Box Recalled for Undeclared Tree Nuts

    Queen Bee Gardens recalls Truffle Dark Gift Box due to undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. The product poses a risk to consumers with tree nut allergies.

    Product
    Truffle Dark Gift Box, 12 pc., 6 oz. PLU Code: 788394 17660 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1486-2022·2022-07-27

    Honeymoons Dark Chocolate Cashew Recalled for Undeclared Tree Nuts

    Honeymoons Dark Chocolate Cashew products may contain undeclared tree nuts including pecans, almonds, coconut, macadamia, and walnuts. The product is being recalled from Queen Bee retail locations in Colorado, New Mexico, Wyoming, and nationwide online.

    Product
    Honeymoons Dark Chocolate Cashew. PLU Code: 788394 14864 4.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1488-2022·2022-07-27

    Honeymoons Milk Chocolate Pecan recalled for undeclared tree nuts

    Queen Bee Gardens is recalling Honeymoons Milk Chocolate Pecan candies due to the potential presence of undeclared tree nuts. Consumers with tree nut allergies should not consume this product.

    Product
    Honeymoons Milk Chocolate Pecan. PLU Code: 788394 14684 8. Ingredients: Honey, milk chocolate (sugar, milk, cocoa butter, chocolate liquor, sunflower lecithin and pure vanilla), pecans, butter (pasteurized cream, salt) cream, nonfat dry milk, whey, sunflower lecithin, algin…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1283-2022·2022-07-27

    FDA Recalls Cipla Difluprednate Eye Drops for Defective Container Caps

    Cipla is recalling 8,136 bottles of Difluprednate ophthalmic emulsion nationwide due to defective container caps that can break and expose the medication tip, compromising sterility.

    Product
    DIFLUPREDNATE — DIFLUPREDNATE (DIFLUPREDNATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1433-2022·2022-07-27

    BD Connecta Stopcock Recalled for Potential Housing Leakage

    Becton Dickinson is recalling approximately 1.96 million BD Connecta Stopcock devices due to potential leakage at the housing component, which could interrupt treatment and expose patients to biohazardous material.

    Product
    BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1498-2022·2022-07-27

    Chocolate Sampler product recalled due to undeclared tree nuts

    Queen Bee Gardens is recalling Chocolate Sampler 13 oz packages due to undeclared tree nuts. The products may contain pecans, almonds, coconut, macadamia nuts, or walnuts.

    Product
    Chocolate Sampler Net wt. 13 oz. PLU Code: 788394 76511 7
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1442-2022·2022-07-27

    Chuckanut Bay Key Lime Cheesecake Bites Recalled for Undeclared Soy

    Chuckanut Bay Foods LLC recalls Key Lime Cheesecake Bites (Item 32012-56, Lot 2C168A2) because the label fails to declare soy lecithin, posing a risk to consumers with soy allergies.

    Product
    Item 32012-56, Chuckanut Bay Key Lime Cheesecake Bites (Dark Compound) BULK. Perishable - Keep Refrigerated. There are 14 pieces per pack and 56 packs per case. The label is read in parts: BUTTER OIL, ENRICHED FLOUR (wheat flour ***), CRYSTALLIZED LIME***, SALT, CAROB BEAN…
    Category
    Food
    Distribution
    13 states
  • HighFDA (Devices)·Z-1443-2022·2022-07-27

    Spinal Fusion Implant Cross Connectors Recalled for Insufficient Clamping Force

    Aesculap is recalling its S4 Cervical Cross Connector used in spinal fusion surgery due to insufficient clamping force that may cause the connectors to move on the rods or shed particles.

    Product
    AESCULAP S4 Cervical Cross Connector L22mm, S4C CROSS CONNECTOR FIXED 22MM, product code SW112T. Used in spinal fusion surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1462-2022·2022-07-27

    Macadamia Classic Truffles Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Macadamia Classic Truffles because they may contain undeclared tree nuts including almonds, coconut, and walnuts. The product poses allergen risks to consumers with tree nut allergies.

    Product
    Macadamia Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11060 3. Ingredients: Milk chocolate (sugar, milk, cocoa butter, chocolate liquor, soya lecithin and pure vanilla) honey, butter (pasteurized cream, salt), cream, roasted & sea salted macadamias, pecans, non-fat dry…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1273-2022·2022-07-27

    Oxytocin Injectable Recalled Due to Lack of Sterility Assurance

    Nephron Sterile Compounding Center is recalling Oxytocin 30 Units/500 mL injectable solution due to lack of sterility assurance. Approximately 1,810 bags with lot codes OX2013C and OX2013E were distributed nationwide.

    Product
    Oxytocin 30 Units/500 mL (0.06 Units/mL) in 0.9% Sodium Chloride Injection, USP IV bag, packaged in 10 x 1 IV Bag per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-543-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1450-2022·2022-07-27

    Chocolate Cheesecake Bites Recalled for Undeclared Soy Lecithin

    Chuckanut Bay Foods is recalling Chocolate Cheesecake Bites because the label lists Sunflower Lecithin when the product actually contains Soy Lecithin, an undeclared allergen. Consumers with soy allergies face a potential health risk.

    Product
    Item 32017-56, Chocolate Cheesecake Bites BULK. Perishable - Keep Refrigerated. There are 14 pieces per pack and 56 packs per case. Firm did not provide label.
    Category
    Food
    Distribution
    13 states
  • HighNHTSA·22V541000·2022-07-27

    2022-2023 BMW IX and i4 High-Voltage Battery Fire Risk Recall

    Certain 2022-2023 BMW IX and 2022 i4 vehicles are recalled due to high-voltage batteries that may develop internal damage and short-circuit, posing a fire risk. Owners should not drive or charge the vehicle until the battery is replaced.

    Product
    BMW — BMW IX, I4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1451-2022·2022-07-27

    Almond Coconut Truffles Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Almond Coconut Classic Truffles for undeclared tree nuts (pecans, almonds, coconut, macadamia, walnuts). The affected product was sold in Colorado, New Mexico, Wyoming, and nationwide online.

    Product
    Almond Coconut Classic Truffle. Net Wt. 1.4 oz. PLU Code: 788394 11025 2. Ingredients: Milk & dark chocolate, honey, butter (pasteurized cream & salt), cream, coconut, almonds, non-fat dry milk, whey, natural flavors, agar, algin & lecithin. Note: Typo on website should be…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1445-2022·2022-07-27

    Chuckanut Bay Cheesecake Bites Recalled for Undeclared Soy Lecithin

    Chuckanut Bay Foods is recalling Dipped Cheesecake Bites Chocolate because the product label lists Sunflower Lecithin when it actually contains undeclared Soy Lecithin, a potential allergen.

    Product
    Item 39417-12, Chuckanut Bay DIPPED CHEESECAKE BITES Chocolate. Perishable - Keep Refrigerated. There are 4 pieces per pack and 12 packs per case. Net Wt. 3.2 oz. per package. UPC 6 03812 39417 8. The label is read in parts: "***INGREDIENTS: CREAM CHEESE***, CANE SUGAR…
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-1440-2022·2022-07-27

    Chuckanut Bay Chocolate Covered Cheesecake Bites Recalled for Undeclared Soy Allergen

    Chuckanut Bay Foods is recalling 18 cases of Chocolate Covered Coconut Cheesecake Bites due to undeclared soy lecithin. The product contains soy lecithin but is labeled as containing sunflower lecithin, posing a risk to allergic consumers.

    Product
    Item 34033-12, Chuckanut Bay Chocolate Covered Coconut Cheesecake Bites. Perishable - Keep Refrigerated. There are 8 pieces per pack and 12 packs per case. Net Wt. 6.4 oz. UPC 6 03812 34033 5. The label is read in parts: "***INGREDIENTS: CREAM CHEESE***, CHOCOLATE COMPOUND…
    Category
    Food
    Distribution
    13 states
  • HighFDA (Drugs)·D-1256-2022·2022-07-27

    HYDROmorphone HCl Injection Syringes Recalled for Sterility Assurance

    Nephron Sterile Compounding Center is recalling HYDROmorphone HCl Injection syringes nationwide due to lack of assurance of sterility. The recall affects 12,900 syringes across two manufacturing lots.

    Product
    HYDROmorphone HCl Injection, USP, 6 mg/30 mL (0.2 mg/mL) syringes, 5 x 30 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: 69374-529-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1456-2022·2022-07-27

    Chocolate Truffles Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Dark on Dark Classic Truffle products due to the potential presence of undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, and walnuts) that pose an allergen risk to sensitive consumers.

    Product
    Dark on Dark Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11030 6. Ingredients: Dark chocolate, honey, butter (pasteurized cream & salt), cream, non-fat dry milk, whey, agar, algin & lecithin.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1249-2022·2022-07-27

    Compounded Injectable Medications Recalled for Sterility Assurance Failure

    Nephron Sterile Compounding Center is recalling 2,315 pre-filled syringes due to lack of sterility assurance. The compounded injectable medication was distributed nationwide.

    Product
    Bupivacaine HCl 150 mg (3.0 mg/mL), Ketorolac Tromethamine 60 mg (1.2 mg/mL), Ketamine HCl 60 mg (1.2 mg/mL) Injection, 50 mL syringes, 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.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1468-2022·2022-07-27

    QBee Sea Salt Caramel Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling QBee Sea Salt Caramel due to undeclared tree nuts. The affected product was sold at ten retail locations in Colorado, New Mexico, and Wyoming, and via internet sales.

    Product
    QBee Sea Salt Caramel. Net wt. 1 oz. PLU Code: 788394 11010 8.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1434-2022·2022-07-27

    BD Connecta Stopcock recalled for potential housing leakage risk

    Becton Dickinson is recalling BD Connecta Stopcocks due to potential leakage at the housing component. The defect may interrupt treatment and expose patients to biohazardous material.

    Product
    BD Connecta Stopcock Without Extension Tube Catalog No. 394602 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1279-2022·2022-07-27

    Sodium Bicarbonate Injection USP recalled for lack of sterility assurance

    Nephron Sterile Compounding Center recalls 36,354 pre-filled syringes of Sodium Bicarbonate Injection due to lack of sterility assurance. The medication was distributed nationwide.

    Product
    8.4% Sodium Bicarbonate Injection, USP, 4.2 g/50 mL (84 mg/mL) 1 mEq/mL syringe, packaged in 1 x 50 mL Pre-Filled Syringe per carton, 30 x 1 syringe carton per case, Rx Only Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-214-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1411-2022·2022-07-27

    Medical Device Recall: Hill-Rom PRO+ Mattress Microclimate Feature Failure

    Hill-Rom PRO+ mattresses are being recalled for a Microclimate Management feature failure that could increase pressure ulcer risk in patients. The recall affects 200 units distributed in the US and Canada.

    Product
    Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress, REF P7924A01; and REF P7924ARENT01, PRO+ MRS Rental Surface with X-Ray mattress.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1444-2022·2022-07-27

    Aesculap S4 Cervical Cross Connector Spinal Implant System Recalled for Clamping Failure

    Aesculap Implant Systems is recalling the AESCULAP S4 Cervical Cross Connector (product code SWT113T) used in spinal fusion surgery. The connectors may not clamp properly onto rods, potentially causing movement and wear particles.

    Product
    AESCULAP S4 Cervical Cross Connector L24mm, S4C CROSS CONNECTOR FIXED 24MM, product code SWT113T. Used in spinal fusion surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide