The Recall Desk

State

Oregon product recalls

73,096 recalls have nationwide distribution and so reach Oregon. 7,529 additional recalls listed Oregon specifically in their distribution scope.

What the numbers show

Total
7,529
Critical
876
Severe
1,805
Most recent
2026-09-23

Of the 7,529 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 1,805 (24%) are Severe.

These figures cover only the 7,529 recalls whose distribution notice names Oregon specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10626–10650 of 80625

  • SevereFDA (Food)·F-1654-2024·2024-08-14

    Al'Fez Natural Tahini Recalled for Potential Salmonella Contamination

    Al'Fez Natural Tahini in 5.6oz glass jars is being recalled due to potential Salmonella contamination. The recall affects 3,522 cases distributed nationwide.

    Product
    Al'Fez Natural Tahini in 5.6oz glass jars, UPC 711464506778
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1668-2024·2024-08-14

    Palmer Frosted Munchy Medley Snack Mix Recalled for Salmonella

    Palmer & Company is recalling Palmer Frosted Munchy Medley snack mix nationwide (US and Canada) due to potential salmonella contamination. Consumers should not eat the product and should discard it or return it to where purchased.

    Product
    Palmer Frosted Munchy Medley, A mixture of Sweet & Salty Favorites, Net Wt 15 oz., UPC 77232 37013, 8/15oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2443-2024·2024-08-14

    Medline Procedure Kits Recalled Due to Defective Plastic Syringes

    Medline procedure kits containing defective plastic syringes are being recalled nationwide. The syringes may leak, break, or have other quality issues that could pose a risk to patient health.

    Product
    Medline procedure kits labeled as: 1) NEPHROLOGY PACK, Pack Number DYNJ59089; 2) NERVE BLOCK TRAY, Pack Number DYNJRA1221A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1661-2024·2024-08-14

    Sunny Select Strawberry Yogurt Coated Pretzels Recalled for Salmonella Risk

    Palmer & Company is recalling Sunny Select Strawberry Yogurt Coated Pretzels (10 oz, UPC 9848796055) distributed nationwide in the US and Canada due to potential salmonella contamination.

    Product
    Sunny Select Strawberry Yogurt Coated Pretzels, Net Wt. 10 oz, UPC 9848796055, 12/10oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1673-2024·2024-08-14

    Costco salad recalled for undeclared almond and soy allergens

    Costco is recalling an Ancient Grain + Vegetable Salad due to undeclared almond and soy allergens. Consumers with these allergies should not consume the product.

    Product
    The recalled product is mis-labeled as Ancient Grain + Vegetable Salad item #25247. Product is perishable, refrigerated, and packaged in clear dome clamshell plastic container. Net weight approximately 2.6 pounds per package. Almond slices are visible through a clear plastic c
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Food)·F-1662-2024·2024-08-14

    Palmer Candy Pretzel Rods recalled for potential salmonella contamination

    Palmer & Company is recalling Palmer Candy Vanilla Chocolatey Swirl Enrobed Pretzel Rods (8 oz) nationwide due to potential Salmonella contamination. Consumers should not consume this product.

    Product
    Palmer Candy Vanilla Chocolatey Swirl Enrobed Pretzel Rods, Crunchy Salted Pretzel Coated with White Fudge and a Fancy Chocolatey Swirl, Net Wt. 8oz, UPC 77232 17011, 12/8oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1658-2024·2024-08-14

    Urge! and Casey's Caramel Pretzels Recalled for Potential Salmonella

    Palmer & Company is recalling Urge! Caramel Swirl Pretzels and Casey's Caramel Swirl Coated Pretzels nationwide due to potential Salmonella contamination.

    Product
    1. Urge! Caramel Swirl Pretzels, White Fudge Coated Pretzel Twists Drizzled in Caramel, Net Wt. 6oz, UPC 39779 00417, 8/6oz case 2. Casey's Caramel Swirl Coated Pretzels, Net Wt. 4 oz., UPC 98437 26082, 6/4oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1672-2024·2024-08-14

    Palmer Patriotic Pretzels recalled for potential salmonella contamination

    Palmer & Company is recalling Palmer Patriotic Pretzels due to potential salmonella contamination. The affected products were distributed nationwide in the United States and Canada.

    Product
    1. Palmer Patriotic Pretzels, White & Chocolatey Fudge Covered Star Shaped Pretzels, Net Wt. 6oz, UPC 77232 37055, 16/6oz case 2. Palmer Patriotic Pretzels, White & Chocolatey Fudge Covered Star Shaped Pretzels, Net Wt 14 oz, UPC 7723237059, 12/14 oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1665-2024·2024-08-14

    Palmer Candy Munchy Medley products recalled due to potential salmonella contamination

    Palmer & Company is recalling multiple Munchy Medley candy and snack products nationwide due to potential salmonella contamination. Salmonella can cause serious illness in vulnerable populations.

    Product
    1. Palmer Candy Munchy Medley, Item 38004, Net Wt. 16/6oz bulk case, UPC 77232 38004 2. Palmer Candy Munch Medley, Item 10737, Net Wt. 15 lbs, UPC 77232 10737 3. Casey's Munchy Medley, Sweet & Salty Crunch Mix, Net Wt. 4.25 oz, UPC 98437 26083 6/case 4. Snackin' with the Crew! Mi
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1667-2024·2024-08-14

    Palmer Candy Chow Down Mix Recalled Due to Potential Salmonella

    Palmer & Company is recalling Palmer Candy Chow Down Mix (Item 10731, 25 lbs, UPC 77232 10731) distributed nationwide in the US and Canada due to potential salmonella contamination.

    Product
    Palmer Candy Chow Down Mix, Item 10731, Net Wt 25lbs, UPC 77232 10731
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1660-2024·2024-08-14

    Patriotic Pretzel Products Recalled for Potential Salmonella Contamination

    Palmer & Company is recalling Freshness Guaranteed Patriotic Red, White & Blue Pretzel Twists and Palmer Candy Frosted Patriotic Pretzels nationwide due to potential salmonella contamination.

    Product
    1. Freshness Guaranteed Patriotic Red, White & Blue Pretzel Twists, Net Wt 14 oz., UPC 78742 03913, 8/14oz case 2. Palmer Candy Frosted Patriotic Pretzels, Item 10757, Net Wt 28 lbs, UPC 77232 10757
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0631-2024·2024-08-14

    Acetaminophen tablets incorrectly labeled with aspirin drug facts information

    Some bottles of Acetaminophen Extra Strength 500 mg tablets are labeled with the drug facts information for Aspirin 81 mg tablets. The affected lot is 4138197 (expiration 10/31/2025), distributed nationwide.

    Product
    ACETAMINOPHEN — ACETAMINOPHEN (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1670-2024·2024-08-14

    Peanut Butter Snack Mix Recalled for Potential Salmonella Contamination

    Palmer & Company is recalling Freshness Guaranteed Peanut Butter Snack Mix due to potential salmonella contamination. The recall affects 12oz and 4.5oz packages distributed nationwide in the United States and Canada.

    Product
    1. Freshness Guaranteed Peanut Butter Snack Mix, Net Wt 12oz, UPC 78742 03912, 8/12oz case 2. Peanut Butter Snack Mix, Net Wt 4.5oz to go container, Distributed by: Kwik Trip Inc; UPC 39779 00424, 12/4.5oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1663-2024·2024-08-14

    Palmer Patriotic Munchy Medley Recalled for Potential Salmonella Contamination

    Palmer & Company is recalling Palmer Patriotic Munchy Medley candy nationwide in the United States and Canada due to potential salmonella contamination.

    Product
    Palmer Patriotic Munchy Medley, Net Wt 15oz, UPC 7723237060, 12/15oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2488-2024·2024-08-14

    BD PYXIS Automated Medication Cabinet Software Label Error Affects 11 Units

    CareFusion's BD PYXIS medication dispensing cabinet with software version 3.9.1.9 may print incorrect bin labels during restocking, potentially leading to wrong medication dispensing. Eleven units distributed nationwide are affected.

    Product
    BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P, REF: 169-82 containing software version 3.9.1.9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2490-2024·2024-08-14

    BD PYXIS automated medication cabinet software defect causes incorrect bin labels

    A software defect in BD PYXIS MEDBANK automated medication dispensing cabinets may cause the incorrect medication bin to be printed on restock labels, potentially resulting in medication errors.

    Product
    BD PYXIS MEDBANK TWR MN CR-12HH-1FH, REF: 169-84 containing software version 3.9.1.9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0630-2024·2024-08-14

    Estradiol Cypionate Injection Recalled Due to Lack of Sterility Assurance

    Empower Pharmacy is recalling Estradiol Cypionate Injection due to lack of assurance of sterility. The recall affects 2,797 units distributed nationwide within the United States.

    Product
    Empower Pharmacy, Estradiol Cypionate Injection, 10mg/mL, 5mL Sterile Multiple Dose Vial, For IM or SQ use only, RX only, Compounded by: Empower Pharmacy 7601 N Sam Houston Pkwy W Ste 100, Houston, TX 77064
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2509-2024·2024-08-14

    Philips IntelliVue Patient Monitors with disabled monitoring software options

    Philips IntelliVue Patient Monitors (MX400/450/500/550) with software versions L.x or M.x lack required monitoring capabilities due to removed software entitlements. The missing features could lead to incorrect or delayed patient treatment.

    Product
    IntelliVue Patient Monitor MX450 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866062. Indicated for use by health care professionals for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, an
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2528-2024·2024-08-14

    Multitom Rax X-Ray Systems Support Arm May Lower Unexpectedly

    The support arm on Siemens Multitom Rax X-ray systems may unintentionally lower, creating a fall risk to people positioned beneath the ceiling-mounted display during system positioning.

    Product
    Multitom Rax -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image Model Number: 10860700
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2533-2024·2024-08-14

    Verigene Gram Positive Blood Culture Test Recalled for Defective Cartridges

    Luminex recalls approximately 1,100 diagnostic kits due to defective test cartridges that may produce false positive results for Staphylococcus lugdunensis and Enterococcus faecium bacteria.

    Product
    Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2511-2024·2024-08-14

    Philips IntelliVue Patient Monitors Shipped with Missing Monitoring Capabilities

    Philips IntelliVue patient monitors shipped or updated with software that removes monitoring capabilities, potentially delaying or resulting in incorrect treatment.

    Product
    IntelliVue Patient Monitor MX550 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866066. Indicated for use by health care professionals for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1669-2024·2024-08-14

    Favorite Day Bakery White Fudge Mini Cookies recalled for salmonella

    Favorite Day Bakery White Fudge Mini Cookies (7oz) recalled nationwide in the US and Canada due to potential salmonella contamination.

    Product
    Favorite Day Bakery White Fudge Mini Cookies, Net Wt 7oz, UPC 85239 92319, 16/7oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2532-2024·2024-08-14

    FDA Recalls CryoPatch Cardiac Tissue Grafts Due to Invalid Test Results

    Artivion has recalled CryoPatch SG cardiac tissue patches used in pulmonary surgeries due to approval and release with invalid test results. Patients who received implants should consult their healthcare provider.

    Product
    (1) CryoPatch SG Pulmonary Human Cardiac Hemi-Artery - Artery Patch, SGPH00 Cryopreserved Decellularized Cardiac Tissue Allograft Prepared with SynerGraft (SG) Technology; and (2) CryoPatch SG Pulmonary Human Cardiac Branch Patch, SGP020, Cryopreserved Decellularized Cardiac Tis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2495-2024·2024-08-14

    BD PYXIS Medication Cabinet Software Defect Causes Incorrect Restock Labels

    A software issue in BD PYXIS automated medication dispensing cabinets can cause restock labels to print with incorrect bin numbers. Four units are affected nationwide.

    Product
    BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P, REF: 169-90 containing software version 3.9.1.9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2514-2024·2024-08-14

    Diagnostic Test Kits Recalled for False Vibrio Results With Certain Transport Medium

    BioFire Diagnostics is recalling gastrointestinal diagnostic test kits due to false positive Vibrio results when used with certain transport mediums.

    Product
    BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0116 (30 test kit) BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0104 (6 kit test) The BIOFIRE FILMARRAY Gastrointestinal (GI) Panel is a qualitative multiplexed nucleic acid-based in vitro diagnost
    Category
    Medical Device
    Distribution
    Distributed nationwide