The Recall Desk

State

Oregon product recalls

73,566 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.

These figures cover only the 7,533 recalls whose distribution notice names Oregon specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27026–27050 of 81099

  • ModerateFDA (Devices)·Z-1565-2021·2021-05-19

    ICU Medical Recalls Oncology Kits Due to Molding Defect and Leakage

    ICU Medical is recalling specific lots of Oncology Kits due to a molding defect that may cause leakage in the inactivated position.

    Product
    REF CH3397 Oncology Kit w/Spiros¿, Red Cap, Bag Spike w/Clave Additive Port LOT 5118610 - Product Usage: for use in the preparation and patient administration of cytotoxic medications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1586-2021·2021-05-19

    ICU Medical Recalls Spinning Spiros Male Luers Due to Molding Defect

    ICU Medical is recalling specific lots of Spinning Spiros male luers because a molding defect may cause small amounts of leakage in the inactivated position.

    Product
    REF 20130-01 Spinning Spiros¿ Closed Male Luer, Red Cap REF CH2000S-PC Spinning Spiros¿ Closed Male Luer, Purple Cap - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1590-2021·2021-05-19

    ICU Medical Recalls Spinning Spiros Male Luers Due to Leakage Defect

    ICU Medical is recalling specific lots of Spinning Spiros Closed Male Luers because a molding defect may cause leakage in the inactivated position.

    Product
    REF K7040-001 Spinning Spiros Closed Male Luer - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted into a vein).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1536-2021·2021-05-19

    Fresenius AquaBplus Water Purification System Recalled for Installation Error

    Fresenius Medical Care is recalling 27 AquaBplus water purification systems because an installation guideline error may reduce the effectiveness of heat disinfection.

    Product
    AquaBplus and AquaBplus B2 Water Purification System - Product Usage: Intended for use with a hemodialysis system to remove organic and inorganic substances and microbial contaminants from the water used for hemodialysis or related therapies. Fresenius P/N 24-2500-0 All 3…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1560-2021·2021-05-19

    Haag-Streit LENSTAR LS900 Software Recall for Data Mixing Errors

    Haag-Streit USA Inc is recalling Eyesuite 9.3.1 software for LENSTAR LS900 devices due to potential mixing of patient names and examination data.

    Product
    Eyesuite 9.3.1 software, LENSTAR, MODEL LS900: ac-powered slit-lamp biomicroscope.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1587-2021·2021-05-19

    ICU Medical Recalls Bag Spike Adapters Due to Molding Defect

    ICU Medical is recalling specific lots of Bag Spike Adapters due to a molding defect that may cause leakage in the inactivated position.

    Product
    REF CH3034 5" (13 cm) Bag Spike Adapter w/Spiros" w/Red Cap, Vented Cap - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted into a vein).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1575-2021·2021-05-19

    ICU Medical Recalls Smallbore Extension Sets Due to Molding Defect

    ICU Medical is recalling specific lots of smallbore extension sets because a molding defect may cause leakage in the inactivated position.

    Product
    REF CL4151 45" (114 cm) Appx 1.7 ml, Smallbore Ext Set w/Spiros w/Red Cap, Anti-Siphon Valve, Clamp, Y-Connector w/ChemoLock Port, Rotating Luer - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1561-2021·2021-05-19

    Remel Bile Esculin Azide Agar Recalled for Growth of E. faecalis

    Remel Inc is recalling Bile Esculin Azide Agar with Vancomycin because the media allows growth of E. faecalis ATCC 29212.

    Product
    Remel Bile Esculin Azide Agar w/ 6mcg/ml Vancomycin, Product #R01186, 10/package - Product Usage: use in qualitative procedures as a screening method for primary isolation and presumptive identification of vancomycin-resistance enterococci (VRE) from surveillance cultures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1589-2021·2021-05-19

    ICU Medical Recalls IV Administration Sets Due to Molding Defect

    ICU Medical is recalling specific lots of IV administration sets because a molding defect may cause leakage in the inactivated position.

    Product
    REF CH3762 35" (89 cm) Appx 3.9 ml, 10 Drop Admin Set w/Integrated Clave" Drip Chamber, Clave", Spiros" w/Red Cap, Bag Hanger - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1562-2021·2021-05-19

    Musculoskeletal Transplant Foundation Recalls AFT Straight Tubes Due to Filling Error

    Musculoskeletal Transplant Foundation is recalling AFT Straight Tubes that were filled only halfway instead of three-quarters, which may cause surgery delays.

    Product
    AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous defects created from traumatic injury. It can be used in the: extremities, pelvis, and spine Item Number: 227007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1563-2021·2021-05-19

    Randox Calibration Serum Level 3 Recalled for Bilirubin Bias

    Randox Laboratories is recalling 98 kits of Calibration Serum Level 3 (CAL 3) due to a positive bias in bilirubin measurements.

    Product
    Calibration Serum Level 3 (CAL 3) - multi-analyte mixture calibrator. Catalogue Number: CAL2351
    Category
    Medical Device
    Distribution
    15 states
  • ModerateFDA (Devices)·Z-1574-2021·2021-05-19

    ICU Medical Recalls Oncology Kits Due to Potential Leakage Defect

    ICU Medical is recalling specific lots of Oncology Kits because a molding defect may cause small amounts of leakage in the inactivated position.

    Product
    REF CL3960 Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros ; w/ChemoLock; Syringe Transfer Set w/MicroClave, w/ChemoLock Port - Product Usage: provides access for the administration of fluids from a container to a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V364000·2021-05-18

    MCI Recalls Diesel Buses Due to Fuel Rail Leak Fire Risk

    Motor Coach Industries is recalling specific 2017-2021 MCI diesel buses because a fuel rail leak could cause a fire.

    Product
    MCI — MCI D4000, J4500, D4505, D4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V365000·2021-05-18

    New Flyer Recalls Buses Due to Fuel Rail Leak Fire Risk

    New Flyer is recalling certain 2016-2021 XD and XDE series buses because a fuel rail leak could cause a fire.

    Product
    NEW FLYER — NEW FLYER XD35, XD60, XD40, XDE60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·018-2021·2021-05-17

    Kraft Heinz Recalls Chef Francisco Soup Due to Undeclared Allergens

    Kraft Heinz is recalling Chef Francisco soup products because they contain undeclared milk and eggs. The mislabeled frozen soup was distributed to foodservice establishments nationwide.

    Product
    Kraft Heinz Foods Company — Kraft Heinz Foods Company Recalls Chef Francisco Soup Product Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V359000·2021-05-17

    Mercedes-Benz Recalls 2020 Sprinter Vans for Door Hinge Screw Issue

    Daimler Vans USA is recalling 2020 Mercedes-Benz Sprinter vans because front door hinge screws may not be tightened properly, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 3500, SPRINTER 4500, SPRINTER 2500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V363000·2021-05-17

    Husqvarna 701 Enduro LR Recalled for Fuel Line Chafe Risk

    KTM is recalling 2020 Husqvarna 701 Enduro LR motorcycles because fuel lines may chafe and leak, increasing fire risk.

    Product
    HUSQVARNA — HUSQVARNA 701 ENDURO LR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V361000·2021-05-17

    2021 Ducati Scrambler Turn Signals May Not Flash Brightly Enough

    Ducati is recalling certain 2021 Scrambler 800 Night Shift motorcycles because the front and rear turn signal lights may not flash brightly enough, reducing visibility to other drivers and increasing crash risk.

    Product
    DUCATI — DUCATI SCRAMBLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V360000·2021-05-17

    Mercedes-Benz Recalls 2019 Sprinter Vans for Stability Control Software Update

    Daimler Vans USA is recalling 2019 Mercedes-Benz Sprinter vans with camper upfits because the Electronic Stability Control software was not updated for their higher center of gravity.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER (VS30)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V362000·2021-05-17

    2021 Porsche Taycan and Panamera Front Suspension Trailing Arm Defect Recall

    Porsche is recalling certain 2021 Taycan and Panamera models due to front lower trailing arms that may not be properly forged and could break, risking loss of vehicle control.

    Product
    PORSCHE — PORSCHE PANAMERA 4S E-HYBRID, PANAMERA 4S, PANAMERA 4 E-HYBRID, PANAMERA TURBO S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V358000·2021-05-17

    Sutphen Recalls One 2012 SP70 Vehicle for Display Lockup Issue

    Sutphen is recalling one 2012 SP70 vehicle because low voltage spikes may cause the LCD display to lock up, potentially delaying emergency efforts.

    Product
    SUTPHEN — SUTPHEN SP70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V352000·2021-05-14

    Gillig Recalls 2017-2020 Low Floor Vehicles Due to Fuel Leak Risk

    Gillig is recalling 2017-2020 Low Floor vehicles because a fuel rail leak could cause a fire. Owners should contact Gillig for a free inspection and repair.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V353000·2021-05-14

    Mercedes-Benz 2019-2021 G63 and G550 Rear Door Latch Defect

    Mercedes-Benz is recalling 2019-2021 G550 and G63 AMG vehicles for defective rear door latches that may not engage properly or open while driving, creating risk of injury or crashes. Dealers will replace the latches free of charge.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G 550, AMG G63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V351000·2021-05-14

    Nova Bus Recalls 2016-2020 LFS Models Due to Fuel Rail Leak Risk

    Nova Bus is recalling 2016-2020 LFS and LFS Artic vehicles because a defective sealing washer may cause high-pressure fuel leaks, increasing fire risk.

    Product
    NOVA BUS — NOVA BUS LFS ARTIC, LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V355000·2021-05-14

    VanLeigh Water Heater Housing Defect May Create Fire Risk

    VanLeigh is recalling certain 2019-2022 Vilano and 2019-2021 Beacon coaches because the water heater housing may not be properly sealed, allowing gas to enter the coach and creating a fire risk.

    Product
    VANLEIGH — VANLEIGH VILANO, BEACON
    Category
    Vehicle
    Distribution
    Distributed nationwide