The Recall Desk

State

Oregon product recalls

73,478 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 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23526–23550 of 81011

  • SevereFDA (Food)·F-0678-2022·2022-02-16

    Dole and Marketside Salad Kits Recalled for Potential Listeria Contamination

    Dole Fresh Vegetables Inc is recalling multiple salad kit products due to potential Listeria monocytogenes contamination. The recall affects Dole, Little Salad Bar, and Marketside branded 12-13 oz kits distributed across 36 states.

    Product
    Dole 13oz Southwest Kit Product UPC 071430017012 Little Salad Bar 12oz Chopped Southwest Kit Product UPC 4099100087031 Marketside 13.4oz Chopped Southwest Kit Product UPC 681131305129
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0667-2022·2022-02-16

    Dole Buffalo Ranch Chopped Kit recalled for potential Listeria contamination

    Dole Fresh Vegetables Inc is recalling Dole 12.1oz Buffalo Ranch Chopped Kit products due to potential Listeria monocytogenes contamination. The recall affects products distributed across 36 states with specific best-if-used-by dates.

    Product
    Dole 12.1oz Buffalo Ranch Chopped Kit Product UPC 071430000946
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0669-2022·2022-02-16

    Dole Chopped Salad Kits Recalled for Potential Listeria Contamination

    Dole and Little Salad Bar chopped salad kits with specific date codes are being recalled due to potential Listeria monocytogenes contamination. Consumers should not eat the affected products.

    Product
    Dole 12.2oz Chopped Sunflower Crunch Kit Product UPC 071430000342 Little Salad Bar 12oz Chop Sunflower Crunch Kit Product UPC 4099100087925
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0689-2022·2022-02-16

    Dole Peppercorn Ranch Chopped Kit recalled for potential Listeria contamination

    Dole Fresh Vegetables is recalling its 9.1oz Peppercorn Ranch Chopped Kit due to potential Listeria monocytogenes contamination. Affected products carry best-if-used-by dates of November 30, 2021 through January 8, 2022.

    Product
    Dole 9.1oz Peppercorn Ranch Chopped Kit Product UPC 071430000939
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0686-2022·2022-02-16

    Dole Spinach Miso Crunch Kit Recalled for Potential Listeria Contamination

    Dole Fresh Vegetables Inc is recalling approximately 2.3 million cases of Dole 8.3oz Spinach Miso Crunch Kit due to potential Listeria monocytogenes contamination. The product was distributed nationwide.

    Product
    Dole 8.3oz Spinach Miso Crunch Kit Product UPC 071430010532
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0716-2022·2022-02-16

    Nature's Promise Organic Baby Kale Recalled for Potential Listeria Contamination

    Dole Fresh Vegetables Inc is recalling Nature's Promise 5oz Organic Baby Kale Clamshell due to potential Listeria monocytogenes contamination. Affected products were distributed across numerous U.S. states.

    Product
    Nature's Promise 5oz Organic Baby Kale Clamshell Product UPC 688267154492
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0645-2022·2022-02-16

    FDA Class I Recall: Dole American Blend Vegetables for Listeria

    Dole Fresh Vegetables is recalling American Blend vegetable products due to potential Listeria monocytogenes contamination. The recall affects over 2 million cases distributed across 35 states.

    Product
    Ahold 12oz American Blend Product UPC 688267011535 Lidl 12oz American Product UPC 4056489210511 Dole 12oz American Blend Product UPC 071430009338
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0654-2022·2022-02-16

    Dole Chopped Bacon Caesar Salad Recalled for Potential Listeria Contamination

    Dole Fresh Vegetables Inc is recalling approximately 2.3 million cases of Dole 10.2oz Chopped Bacon Caesar salad due to potential Listeria monocytogenes contamination. Affected products were distributed nationwide with Best if Used By dates between November 2021 and January 2022.

    Product
    Dole 10.2oz Chopped Bacon Caesar Product UPC 071430000892
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0682-2022·2022-02-16

    Dole and Kroger Packaged Romaine Products Recalled for Potential Listeria

    Dole Fresh Vegetables Inc is recalling multiple packaged romaine lettuce products due to potential Listeria monocytogenes contamination. The products were distributed across 37 states.

    Product
    Dole 15oz Family Classic Romaine Product UPC 071430010372 Dole 9.0oz Premium Romaine Product UPC 071430009109 Dole 9oz Classic Romaine Product UPC 071430010693 Dole 9oz Hearts of Romaine Product UPC 071430009567 Kroger 10oz Hearts of Romaine Product UPC 011110910448…
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0717-2022·2022-02-16

    Natures Promise Organic Baby Spring Mix Recalled for Potential Listeria

    Dole Fresh Vegetables Inc is recalling Natures Promise 5oz Organic Baby Spring Mix Clamshell due to potential Listeria monocytogenes contamination. Affected products bear codes beginning with 'N' or 'Y' with Best if Used By dates from November 30, 2021 through January 8, 2022.

    Product
    Natures Promise 5oz Organic Baby Spring Mix Clamshell Product UPC 688267154546
    Category
    Food
    Distribution
    36 states
  • HighFDA (Devices)·Z-0595-2022·2022-02-16

    GE Healthcare MR Magnets Cryogenic Ventilation System Defect Recall

    GE Healthcare is recalling 17,228 MR superconducting magnet systems because the cryogenic ventilation system may not meet required venting standards.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA PET/MR System, tomographic imager combining emission computed tomography with nuclear magnetic resonance system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0584-2022·2022-02-16

    KWIK-STIK Quality Control Sets recalled for potential bacterial contamination

    Microbiologics Inc is recalling KWIK-STIK QC Sets and Panels due to potential contamination with E. coli and Staphylococcus species. The affected product was distributed worldwide to laboratory testing facilities.

    Product
    QC Sets and Panels: KWIK-STIK" 2 Pack. Common Name: QC Sets and Panels GP Comprehensive QC Set. Each KWIK-STIK unit contains a lyophilized microorganism pellet, an ampoule of hydrating fluid, and an inoculating swab. Each device is sealed within a laminated pouch that…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0562-2022·2022-02-16

    Novalung Sensor Box Communication Failure May Disable Flow Measurement

    The Novalung Sensor Box may experience communication failures between its flow sensor and sensor box component, potentially disabling flow measurement and air bubble detection. The recall affects 115 units distributed across 16 US states.

    Product
    Novalung Sensor Box (F30000163) a component of Novalung Console (F30000162)- Indicated for long-term (> 6 hours) respiratory/ cardiopulmonary support that provides assisted extracorporeal circulation and physiologic gas exchange (oxygenation and CO2 removal) of the patient's…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0635-2022·2022-02-16

    Acufex Access Advanced Positioning Kit Recalled for Missing Sterilization

    Smith & Nephew is recalling the Acufex Access Advanced Positioning Kit because the products were shipped to a distribution center instead of the sterilizer and were not sterilized before distribution.

    Product
    Acufex Access Advanced Positioning Kit - indicated for use to position and distract the extremity of patient during open and arthroscopic surgical procedures Product Number: 72205104
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0602-2022·2022-02-16

    GE Healthcare MRI systems recalled for cryogen ventilation system defect

    GE Healthcare Discovery MR450 MRI systems may have cryogen ventilation systems that do not meet required venting standards. The recall affects approximately 17,228 devices distributed in the U.S. and internationally.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare Discovery MR450 1.5T system, nuclear magnetic resonance imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0604-2022·2022-02-16

    GE Healthcare MR Superconducting Magnets Recalled for Ventilation Defect

    GE Healthcare recalled 17,228 superconducting magnets, a component of SIGNA 1.5T MR systems, due to a cryogen ventilation system that may not meet venting requirements. Systems are distributed nationwide and internationally.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA 1.5T TwinSpeed MR System, nuclear magnetic resonance system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0596-2022·2022-02-16

    GE Healthcare MRI Systems Recalled for Potential Cryogen Ventilation Defect

    GE Healthcare is recalling approximately 17,228 SIGNA Creator and Explorer MRI systems due to potential defects in their cryogen ventilation systems that may not meet required venting standards.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Creator and SIGNA Explorer System, nuclear magnetic resonance imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0594-2022·2022-02-16

    GE Healthcare MRI Systems Recalled for Inadequate Cryogen Ventilation

    GE Healthcare is recalling MRI superconducting magnets with cryogen ventilation system defects not meeting safety requirements. The recall affects 17,228 devices distributed across the US and internationally.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare Discovery MR750 3.0T System, nuclear magnetic resonance imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0605-2022·2022-02-16

    GE Healthcare MR system magnets recalled due to cryogen ventilation defect

    GE Healthcare is recalling 17,228 MR superconducting magnet components due to a cryogen ventilation system that may not meet required venting specifications.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Infinity MR System, SIGNA Infinity MR System with Excite Technology, nuclear magnetic resonance imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0586-2022·2022-02-16

    Diagnostic Control Microorganism Recalled for Incorrect Test Results

    Diagnostic control microorganisms manufactured by Microbiologics Inc are recalled for returning incorrect antibiotic susceptibility test results. These controls failed quality specifications and could cause inaccurate lab test results.

    Product
    LYFO-DISK Enterococcus faecalis derived from ATCC 51299 In Vitro Diagnostic Control microorganisms
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0565-2022·2022-02-16

    MIC Percutaneous Endoscopic Gastrostomy Kits Recalled for Oversized Retention Bolster

    Avanos Medical is recalling the MIC Percutaneous Endoscopic Gastrostomy (PEG) Kit because the external retention bolster may be oversized relative to the tube. Approximately 2,652 units have been distributed in the US, Canada, and Chile.

    Product
    MIC* Percutaneous Endoscopic Gastrostomy PEG Kit - 20 Fr-PULL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0593-2022·2022-02-16

    GE Healthcare MRI Systems Cryogen Ventilation System Defect Recall

    GE Healthcare is recalling Discovery MR750w 3.0T MRI systems due to cryogen ventilation systems that may not meet FDA venting requirements. Approximately 17,228 devices were affected.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare Discovery MR750w 3.0T System, nuclear magnetic resonance imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0730-2022·2022-02-16

    Amy's Vegan Rice Mac & Cheese Recall: Undeclared Milk Allergen

    Amy's Kitchen is recalling its Vegan Organic Rice Mac & Cheese due to undeclared milk detected during testing. The product is labeled dairy-free, posing a risk to consumers with milk allergies.

    Product
    Amy's Vegan Organic Rice Mac & Cheese; frozen; 8 oz. (227 g) individually packaged serving; in trays with plastic overwrap, inside preprinted cardboard boxes; UPC 04227200432; Amy's Kitchen, Inc., P.O.Box 7129, Petaluma, CA 94955 8 or 12 retail units per case; Organic Gluten…
    Category
    Food
    Distribution
    33 states
  • HighFDA (Devices)·Z-0634-2022·2022-02-16

    Universal Chuck Surgical Instrument Handle May Detach and Release Ball Bearings

    The Universal Chuck instrument handle may loosen and release ball bearings onto the surgical field. If not recovered, these bearings could delay surgery and potentially cause infection or tissue damage.

    Product
    Universal Chuck-The Universal Chuck is an Instrument Handle provided as an alternative instrument available for use in the TN-ADVANCED" Tibial Nailing System (TNA), TFN-ADVANCED" Proximal Femoral Nailing System (TFNA), RFN-ADVANCED" Retrograde Femoral Nailing System (RFNA)…
    Category
    Medical Device
    Distribution
    Distributed nationwide