The Recall Desk

State

Oregon product recalls

73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26201–26225 of 81042

  • HighFDA (Devices)·Z-2013-2021·2021-07-14

    Randox RX Imola Analyzer Software Freeze Recall - 50 Units Affected

    Randox recalls 50 RX Imola Analyser units nationwide and in Puerto Rico due to software freezing that prevents test results from displaying.

    Product
    Randox RX Imola Analyser with ISE, Catalog Numbers RX4900, RX4900R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2043-2021·2021-07-14

    CoreValve Evolut PRO PLUS Delivery Catheter Systems recalled for actuator separation

    Medtronic is recalling CoreValve Evolut PRO PLUS Delivery Catheter Systems due to reports of actuator separation that could affect proper deployment of these cardiac devices.

    Product
    CoreValve Evolut PRO PLUS Delivery Catheter System, REF: D-EVPROP2329US; D-EVPROP34US;
    Category
    Medical Device
    Distribution
    48 states
  • HighFDA (Devices)·Z-2032-2021·2021-07-14

    Nonsterile Femoral Angiography Drapes Recalled Due to Sticking Plastic Film Defect

    Cardinal Health is recalling 26,250 units of Nonsterile Femoral Angiography Drapes due to a manufacturing defect causing the drapes to stick and preventing proper application. This may compromise surgical site protection.

    Product
    Nonsterile Femoral Angiography Drape with Single Pouch, Catalog Number 29525N - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2042-2021·2021-07-14

    Medtronic CoreValve Evolut PRO Delivery Catheter Actuator Separation Recall

    Medtronic is recalling 67,339 CoreValve Evolut PRO Delivery Catheter Systems manufactured before July 11, 2020, due to reports of actuator separation that could affect device function.

    Product
    CoreValve Evolut PRO Delivery Catheter System, REF: ENVPRO-14; ENVPRO-16;
    Category
    Medical Device
    Distribution
    48 states
  • HighFDA (Devices)·Z-2038-2021·2021-07-14

    Angiography and Cesarean Birth Drapes recalled due to sticking defect

    Cardinal Health is recalling Nonsterile Femoral Angiography and Cesarean Birth Drapes (15,360 units) because plastic film causes sticking that may prevent proper unfolding and application.

    Product
    Nonsterile Femoral Angiography Drape, Catalog Numbers: a) 29460NB, b) 29456NB - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0770-2021·2021-07-14

    Beech-Nut Single Grain Rice Baby Cereal Recalled for Elevated Arsenic Levels

    Beechnut Nutrition is recalling Beech-Nut brand Single Grain Rice Baby Cereal because certain lots may contain inorganic arsenic above safe levels. Consumers with affected products should stop use and contact the manufacturer.

    Product
    Beech-Nut brand Single Grain Rice Baby Cereal; NET WT. 8 OZ (227g); INGREDIENTS: Rice flour, sunflower lecithin; packaged in an 8oz plastic canister with safety seal, screw on inner cap and an over cap.
    Category
    Food
    Distribution
    29 states
  • ModerateFDA (Drugs)·D-0651-2021·2021-07-14

    Xylocaine Lidocaine Injection Recalled for Low Epinephrine Assay Results

    Fresenius Kabi USA LLC is recalling Xylocaine-MPF with Epinephrine 1:200,000 injection vials nationwide due to low out-of-specification results for epinephrine assay.

    Product
    XYLOCAINE — XYLOCAINE (LIDOCAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateCPSC·21163·2021-07-14

    Academy Sports Ozone 500 24-Inch Bicycles Recalled for Fall Hazard

    Academy Sports + Outdoors is recalling about 3,860 Ozone 500 Girls' and Boys' Elevate 24-Inch Bicycles because the rear shock spring can become stuck, creating a pinch point and posing a fall hazard to riders.

    Product
    Ozone 500® Girls' and Boys' Elevate 24-Inch Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2031-2021·2021-07-14

    Sterile Femoral Angiography Drape Sticks; Cannot Unfold Properly

    Cardinal Health is recalling 574 units of Sterile Femoral Angiography Drapes because the plastic film causes the drapes to stick, preventing proper unfolding and application during surgery.

    Product
    Sterile Femoral Angiography Drape with Single Pouch, Catalog Number 29525 - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0650-2021·2021-07-14

    Genentech Xolair Injection Recalled for Failed Stability Specifications

    Genentech is recalling two lots of Xolair (omalizumab) injection nationwide due to out-of-specification Polysorbate 20 content detected at the 12-month stability testing timepoint. The affected lots are 3352758 and 3352759, both with August 2021 expiration dates.

    Product
    XOLAIR — XOLAIR (OMALIZUMAB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0786-2021·2021-07-14

    Hatch Verde Salsa Recalled for Potential Foreign Material

    Heritage Family Specialty Foods, Inc. is recalling Hatch Verde Salsa Medium (12 oz jars) due to potential foreign material contamination. The recall affects 646 cases distributed nationwide.

    Product
    Hatch Verde Salsa Medium Net Wt. 12 oz (340g) 6 jars per case packaged in clamshell container UPC Code: 810041591999
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0787-2021·2021-07-14

    Taco Casa Green Salsa Recalled for Potential Foreign Material

    Heritage Family Specialty Foods is recalling Taco Casa Green Salsa due to potential foreign material contamination. The affected product was distributed nationwide.

    Product
    E6164J2 Taco Casa Green Salsa 8 x 4 lb (1.8 kg) pouches
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateCPSC·21164·2021-07-14

    Walgreens Recalls Disney Baby Winnie the Pooh Rattle Sets for Choking Hazard

    Walgreens is recalling about 54,000 Disney Baby Winnie the Pooh Rattle Sets because the feet can detach and pose a choking hazard to young children. Consumers should immediately remove the rattle from children and contact Walgreens for a refund.

    Product
    Disney Baby Winnie the Pooh Rattle Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2012-2021·2021-07-14

    ACE Control Set stability claim failure requires updated handling instructions

    Sentinel CH SpA is recalling ACE Control Set diagnostic control kits due to stability claims after reconstitution that do not meet specified requirements. Updated handling instructions have been provided to affected users.

    Product
    ACE Control Set - IVD Control set for the quantitative determination of Angiotensin Converting Enzyme (ACE) REF 1667001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V529000·2021-07-13

    Entegra and Jayco recreational vehicles recalled for window adhesive failure

    Jayco is recalling certain 2019-2021 recreational vehicles with Hehr 6400 series windows due to adhesive failure. The window vent may detach, increasing the risk of crash or injury.

    Product
    ENTEGRA — ENTEGRA, JAYCO ANTHEM, ASPIRE, INSIGNIA, CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E063000·2021-07-13

    Cummins Recalls L9 Diesel Engines Due to Fuel Hose Leak Risk

    Cummins is recalling specific L9 Diesel Engines equipped with remote Stage 2 fuel filters because a fuel leak may occur from the hose between the fuel pump and filter head.

    Product
    FUEL SYSTEM, DIESEL:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V530000·2021-07-13

    Micro Bird Recalls School Buses Due to Emergency Door Defect

    Micro Bird is recalling 2003-2022 school buses because the service door emergency release handle may bind, preventing evacuation in an emergency.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS, MB II SCHOOL BUS, T-SERIES SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V531000·2021-07-13

    Micro Bird Transit Buses Recalled for Service Door Emergency Release Defect

    Micro Bird is recalling 1,323 transit buses because the service door emergency release handle may bind, preventing evacuation in an emergency.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS, MB II TRANSIT BUS, T-SERIES TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V526000·2021-07-12

    Mercedes-Benz Recalls 2020 GLB 250 for Electrical Fire Risk

    Mercedes-Benz is recalling 2020 GLB 250 vehicles because an incorrect voltage converter socket may cause excessive voltage in the second-row power outlet, increasing fire risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V527000·2021-07-12

    2021 Mercedes-Benz side crash sensor connector defect affects airbag deployment

    Mercedes-Benz is recalling certain 2020-2021 models because side crash sensor connectors may come loose, delaying airbag and seatbelt activation during side impact crashes. Dealers will inspect and replace sensors at no cost.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ S 560, GLC 300, AMG GLC63, G 550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V523000·2021-07-09

    Recreational vehicles recalled for defective window adhesive on multiple models

    Forest River and Coachmen recreational vehicles with Hehr 6400 Series windows are being recalled due to adhesive failure that may cause window vents to detach. Detachment increases the risk of crashes and injuries.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN CEDAR CREEK, GEORGETOWN, SPORTSCOACH, CROSS COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V524000·2021-07-09

    Hyundai Santa Fe and Sonata recalled for fuel pipe leak fire risk

    Fuel may leak at a pipe connection in affected 2021-2022 Hyundai Santa Fe and Sonata vehicles with 2.5L engines, increasing fire risk.

    Product
    HYUNDAI — HYUNDAI SONATA, SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V525000·2021-07-09

    2021 Nissan Rogue Sport Liftgate Hinges May Separate in Rear Crashes

    Nissan is recalling 2021 Rogue Sport vehicles because liftgate hinges may separate during rear-end crashes, compromising door retention. Dealers will replace the hinges free of charge.

    Product
    NISSAN — NISSAN redundant ROGUE SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide