The Recall Desk

State

Oregon product recalls

73,187 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 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13776–13800 of 80716

  • HighUSDA FSIS·PHA-01182024-01·2024-01-18

    USDA Issues Public Health Alert for Uninspected Raw Frozen Pork Dumplings

    USDA FSIS issued a public health alert for raw frozen pork dumplings produced without federal inspection. No illnesses have been reported, but consumers are urged to discard the products.

    Product
    Dim Sum Factory, Inc. — FSIS Issues Public Health Alert for Raw Frozen Pork Dumpling Products Produced without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·24V025000·2024-01-18

    2023 and 2024 Kia Carnival vehicles recalled for loose roof molding

    Kia is recalling certain 2023–2024 Carnival and 2023–2024 Sportage vehicles because the roof molding may loosen and detach, creating a road hazard for other vehicles.

    Product
    KIA — KIA CARNIVAL, SPORTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24086·2024-01-18

    Steamist Wall-Mounted Tilt-Up Bath Shower Seats Recalled for Fall and Laceration Hazards

    Steamist is recalling about 3,900 wall-mounted, folding teak wood shower seats because the support rods and mounting brackets can corrode and break, creating fall and laceration hazards. The firm has received 62 reports of the seats breaking, including 4 injury reports.

    Product
    Tilt-Up Bath & Shower Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0696-2024·2024-01-17

    Eban's Bakehouse cookies recalled for undeclared milk and soy allergens

    Eban's Bakehouse Sweet Indulgences Brown Butter Snickerdoodles are recalled due to undeclared milk and soy allergens. The FDA Class I recall affects 876 units distributed to 33 states.

    Product
    Eban's Bakehouse Sweet Indulgences - Brown Butter Snickerdoodle (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0697-2024·2024-01-17

    Eban's Bakehouse Cookies Recalled for Undeclared Milk and Soy Allergens

    Eban's Bakehouse has recalled Sweet Indulgences Chocolate Chili Coconut cookies due to undeclared milk and soy allergens. The product was distributed nationwide and poses a risk to allergic consumers.

    Product
    Eban's Bakehouse Sweet Indulgences - Chocolate Chili Coconut (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0700-2024·2024-01-17

    Eban's Bakehouse Turtle Brownie Cookies Recalled for Undeclared Milk and Soy

    Eban's Bakehouse LLC is recalling Turtle Brownie cookies that contain undeclared milk and soy allergens. Consumers with allergies should not consume the product.

    Product
    Eban's Bakehouse Sweet Indulgences - Turtle Brownie (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0695-2024·2024-01-17

    Eban's Bakehouse Cookies Recalled for Undeclared Milk and Soy Allergens

    Eban's Bakehouse Sweet Indulgences cookies are being recalled due to undeclared milk and soy allergens. Consumers with allergies should not consume these products and should discard or return them.

    Product
    Eban's Bakehouse Sweet Indulgences - Brown Butter Honey Pistachio (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0699-2024·2024-01-17

    Eban's Bakehouse Cookies Recalled for Undeclared Milk and Soy Allergens

    Eban's Bakehouse Sweet Indulgences cookies are recalled due to undeclared milk and soy allergens not listed on the label. Consumers with allergies to milk or soy should not consume this product.

    Product
    Eban's Bakehouse Sweet Indulgences - Peanut Butter Chocolate Chunk (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-0698-2024·2024-01-17

    Eban's Bakehouse Lemon Sugar Cookies Recalled for Undeclared Milk and Soy

    Eban's Bakehouse Sweet Indulgences lemon cookies are being recalled due to undeclared milk and soy allergens. Consumers with allergies to these ingredients should not consume the product.

    Product
    Eban's Bakehouse Sweet Indulgences - Lemon Sugar Cookie/Lemon Shortbread (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Drugs)·D-0220-2024·2024-01-17

    Prescription Vigabatrin Powder Recalled for Defective Container Leakage Risk

    InvaGen Pharmaceuticals recalls Vigabatrin for Oral Solution nationwide due to defective containers that may leak. Consumers with affected lot should contact their pharmacy or healthcare provider.

    Product
    VIGABATRIN — VIGABATRIN (VIGABATRIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V020000·2024-01-17

    Morgan Super 3 motorcycles recalled for brake master cylinder weld defect

    Morgan Motor Company is recalling 2023 Super 3 motorcycles because a defective weld may cause brake failure. Owners should contact the manufacturer for a free repair.

    Product
    MORGAN MOTOR COMPANY — MORGAN MOTOR COMPANY SUPER 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0694-2024·2024-01-17

    Eban's Bakehouse Sweet Indulgences cookies recalled for undeclared milk and soy

    Eban's Bakehouse LLC is recalling Sweet Indulgences cookies for containing undeclared milk and soy allergens, which pose serious health risks to allergic consumers.

    Product
    Eban's Bakehouse Sweet Indulgences - Variety Pack (12 pieces/cookies) packaged in 11.85oz cardboard candy box with clear plastic cover. Retail sales are by box, Wholesale are 6 boxes per case.
    Category
    Food
    Distribution
    33 states
  • HighFDA (Devices)·Z-0691-2024·2024-01-17

    VISERA Cysto-Nephro Videoscope Model CYF-V2: Reusable Brush Cleaning Update

    Olympus is updating instructions for the VISERA Cysto-Nephro Videoscope (Model CYF-V2) nationwide, removing reusable brushes from manual cleaning procedures. Single-use brushes remain compatible.

    Product
    Model No. CYF-V2, VISERA Cysto-Nephro Videoscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0643-2024·2024-01-17

    Bard Mission Biopsy Instrument Kits Recalled for Improper Needle-Cannula Fit

    Bard is recalling Mission Disposable Core Biopsy Instrument Kits due to dimensional issues that may prevent the biopsy needle from fitting properly into the cannula, potentially causing tissue injury and prolonging procedures.

    Product
    Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit 14G x 16CM; 1610MSK/ Mission Kit 16G x 10CM; 1616MSK/ Mission Kit 16G x 16CM; 1810MSK/ Mission Kit 18G x 10CM; 1816MSK/ Mission Kit 18G x 16CM; 1820MSK/ Mission…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0672-2024·2024-01-17

    SPRYSTEP VECTOR KAFO ankle-foot orthosis recalled for structural failure risk

    The SPRYSTEP VECTOR KAFO custom ankle-foot orthosis is being recalled by Townsend Design due to air pockets that could cause complete structural failure.

    Product
    SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX
    Category
    Medical Device
    Distribution
    48 states
  • HighFDA (Devices)·Z-0714-2024·2024-01-17

    Ambu aView 2 Monitor recalled for fire and burn hazard from oversized mounting screws

    Ambu is recalling the aView 2 A Monitor due to fire and burn hazards if mounting screws longer than 16mm are used. Improper installation can penetrate the lithium-ion battery, causing fires, severe burns, and smoke inhalation.

    Product
    Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0697-2024·2024-01-17

    Olympus ENDOEYE HD II Videoscope Image Discoloration Recall

    Two Olympus ENDOEYE HD II Rigid Videoscope catalog numbers (WA50040A, WA50042A) have been recalled due to reports of pink or green image discoloration during use. The issue could require device exchange during surgery and potentially result in visual impacts or bleeding.

    Product
    Olympus ENDOEYE HD II Rigid Videoscope Catalog Numbers: WA50040A, WA50042A -used with a video system center, light source, documentation equipment, monitor, hand instruments, electrosurgical unit, and other ancillary equipment for endoscopy and endoscopic surgery within the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V018000·2024-01-17

    Heartland Recalls 2024 Corterra Fifth Wheels for Incorrect Tire Labels

    Heartland is recalling 2024 Corterra fifth wheels because certification labels may have missing or incorrect tire size information, potentially leading to the installation of wrong tires.

    Product
    HEARTLAND — HEARTLAND CORTERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0698-2024·2024-01-17

    Medtronic Percutaneous Surgical Pins Recalled Due to Potential Fitting Defects

    Medtronic is recalling 4,235 percutaneous surgical pins that may have a manufacturing defect preventing proper fit into or removal from the tap cap. The pins were distributed nationwide and internationally.

    Product
    Medtronic, REF 9733235, Pin, 100mm, STERILE, PERCUTANEOUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0677-2024·2024-01-17

    Philips BrightView Gamma Camera System Recalled for Extremity Entrapment Hazard

    Philips is recalling BrightView Gamma Camera Systems because a gap can form between patient support and detector during quality assurance scans, creating an extremity entrapment hazard that may cause fractures or crush injuries.

    Product
    BrightView, Gamma Camera System, Product Code 882480.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0640-2024·2024-01-17

    Philips Incisive CT Scanner Software Issues May Cause Misdiagnosis

    Philips is recalling Incisive CT scanners due to nine software defects including image artifacts, incorrect orientation labels, display failures, and positioning errors that could lead to misdiagnosis or need for rescans. No illnesses have been reported.

    Product
    Incisive CT, model 728143 & 728144 running Software Version 5.0.0.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0641-2024·2024-01-17

    Medical diagnostic reagent recall: incorrect cell staining fluorescence

    BD Biosciences is recalling CD11b APC diagnostic reagent vials that may produce dim fluorescence signals, potentially causing false negative results and misdiagnosis of blood cancers.

    Product
    CD11b APC: ASR, REF: 340936, and CE, REF: 333143
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0644-2024·2024-01-17

    Olympus ENDOEYE Videoscope Recalled for Reprocessing Instructions Deviations

    Olympus Corporation recalls 1,403 ENDOEYE Flex endoscopic videoscopes due to deviations in reprocessing instructions. Affected devices may not be reprocessed properly for safe reuse in surgical procedures.

    Product
    OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (5.4 mm diameter) Model: LTF-S190-5 Used with a video system center, light source, documentation equipment, monitor, hand instruments, electrosurgical unit, and other ancillary equipment for endoscopy and endoscopic surgery…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0652-2024·2024-01-17

    Abiomed Introducer Kit Sterile Barrier Compromise Due to Pouch Defect

    Abiomed Introducer Kits may have holes in outer pouches that compromise sterility, exposing patients to bacterial contamination and risk of infection, bacteremia, or sepsis.

    Product
    Abiomed Kit, 14Fr Introducer, 13cm&25cm, Sterile Part of Pump Set (0048-0040, 0048-0045, 1000080)-Introducer(s) are intended for introduction of the Impella Catheter into the body. Part Number: 0052-3046
    Category
    Medical Device
    Distribution
    Distributed nationwide