The Recall Desk

State

Oregon product recalls

73,376 recalls have nationwide distribution and so reach Oregon. 7,531 additional recalls listed Oregon specifically in their distribution scope.

What the numbers show

Total
7,531
Critical
876
Severe
2,128
Most recent
2026-10-07

Of the 7,531 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 7,531 recalls whose distribution notice names Oregon specifically. The 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20326–20350 of 80907

  • HighFDA (Devices)·Z-1684-2022·2022-09-14

    Early Bird Bleed Monitoring System Introducer fails to power on

    Saranas, Inc. is recalling 953 units of the Early Bird Bleed Monitoring System Introducer Sheath Set due to a design error that prevents the device from powering on and completing self-tests. The product was distributed nationwide.

    Product
    Early Bird Bleed Monitoring System Introducer Sheath Set, REF: FG001-01 (6F), FG001-02 (8F)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1488-2022·2022-09-14

    Diphenhydramine Solution Recalled Due to Manufacturing Control Deviations

    Plastikon Healthcare LLC is recalling Diphenhydramine HCl Oral Solution nationwide due to manufacturing control deficiencies that did not meet Current Good Manufacturing Practice standards.

    Product
    Diphenhydramine HCl Oral Solution 12.5 mg / 5 mL, 5 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-6740-70
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1487-2022·2022-09-14

    Calcium Carbonate Oral Suspension Recalled Due to Manufacturing Control Deviations

    Plastikon Healthcare recalls 49,280 cups of Calcium Carbonate Oral Suspension (1250 mg/5 mL) distributed nationwide due to manufacturing process control failures during production.

    Product
    CALCIUM CARBONATE ORAL SUSPENSION, 1250 mg/5 mL, 5 mL cup, packaged in 10 cups per tray, 4 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-7098-94
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1661-2022·2022-09-14

    Handheld ultraviolet-C germicidal wand recalled for excessive radiation

    MERCHSOURCE LLC is recalling a handheld ultraviolet-C germicidal wand (model 1013622) due to excessive ultraviolet-C radiation emission. Consumers should stop using the product immediately.

    Product
    The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1676-2022·2022-09-14

    Laboratory diagnostic system may report inaccurate results during shutdown

    The VITROS XT 7600 laboratory analyzer may report inaccurate test results when the system performs a shutdown. The issue affects approximately 1,148 units distributed worldwide.

    Product
    VITROS XT 7600 Integrated System with Version 3.7.2 and below Product Code: 6844461
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1675-2022·2022-09-14

    VITROS XT 3400 Chemistry System May Produce Inaccurate Test Results

    The VITROS XT 3400 Chemistry System may produce inaccurate test results during shutdown due to electrical current shifts. The FDA has classified this Class II recall, affecting 506 units distributed worldwide.

    Product
    VITROS XT 3400 Chemistry System with Version 3.7.2 and below Product Code: 6844458
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1683-2022·2022-09-14

    Medline Chest Tube Kit Recalled for Non-Sterile Tape Component

    Medline Industries is recalling Chest Tube Convenience Kits due to non-sterile tape included in the sterile portion of the kit, creating a contamination and infection risk.

    Product
    Medline CHEST TUBE REORDER NO: DYNJ36762A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V685000·2022-09-14

    2022 Ford Ranger Loose Fuel Line Connection Increases Fire Risk

    Ford is recalling certain 2022 Ranger and Explorer models with 2.3L engines due to potentially loose fuel line connections. An improperly tightened connection may result in a fuel leak, increasing the risk of fire.

    Product
    FORD — FORD EXPLORER, RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1480-2022·2022-09-14

    FDA Recalls Milk of Magnesia USP for Manufacturing Control Deviations

    Plastikon Healthcare LLC is recalling 502,600 cups of Milk of Magnesia USP due to manufacturing process control deviations. Consumers should discontinue use and consult their healthcare provider if concerned.

    Product
    MILK OF MAGNESIA USP, 2400 mg/30 mL, Magnesium Hydroxide, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6846-73.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1483-2022·2022-09-14

    Magnesium Hydroxide and Aluminum Hydroxide Oral Suspension Recalled for Manufacturing Control Issues

    Plastikon Healthcare LLC is recalling an antacid oral suspension due to manufacturing control deviations. No illnesses have been reported.

    Product
    Magnesium Hydroxide 2400 mg, Aluminum Hydroxide 2400 mg, Simethicone 240 mg MAX, per 30 mL Oral Suspension, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1481-2022·2022-09-14

    Milk of Magnesia Recalled for Manufacturing Process Control Issues

    Plastikon Healthcare LLC is recalling Milk of Magnesia USP due to manufacturing process control deviations affecting approximately 92,200 cups distributed nationwide.

    Product
    MILK OF MAGNESIA USP, 2400 mg/10 mL, Magnesium Hydroxide, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6840-72.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1485-2022·2022-09-14

    Acetaminophen Oral Solution Recalled Due to Manufacturing Control Deviations

    Plastikon Healthcare LLC is recalling Acetaminophen Oral Solution nationwide because manufacturing quality controls were not adequately maintained. Affected product was distributed to institutional healthcare settings.

    Product
    Acetaminophen Oral Solution, 325 mg / 10.15 mL, 10.15 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-6739-71
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1482-2022·2022-09-14

    Antacid Suspension Recalled Due to Manufacturing Process Control Deviations

    Plastikon Healthcare LLC is recalling multiple lots of antacid suspension because manufacturing processes were not adequately controlled. The product was distributed nationwide to institutions.

    Product
    Magnesium Hydroxide 1200 mg, Aluminum Hydroxide 1200 mg, Simethicone 120 mg per 30 mL, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6838-73
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V683000·2022-09-13

    BMW Recalls 2022 745E Hybrid Vehicles Due to Battery Fire Risk

    BMW is recalling one 2022 745E hybrid vehicle because an improperly sized battery cell electrode may cause a short-circuit and increase the risk of fire.

    Product
    BMW — BMW 745E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V679000·2022-09-12

    Mercedes-Benz Recalls 2021 GLB 250 Vehicles Due to Electrical Fire Risk

    Mercedes-Benz is recalling 2021 GLB 250 vehicles because a damaged Electronic Stability Program unit may cause an electrical short circuit, increasing the risk of fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V681000·2022-09-12

    Commercial Trucks Recalled for Steering Shaft Component Failure

    Daimler Trucks North America is recalling 2022-2023 Western Star 47X and 49X commercial trucks because the steering shaft's u-joint pinch bolt may detach, causing loss of steering control.

    Product
    WESTERN STAR — WESTERN STAR 49X, 47X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V678000·2022-09-12

    Mercedes-Benz Recalls 2022 C 300 Vehicles for Electrical Short Risk

    Mercedes-Benz is recalling 2022 C 300 vehicles because moisture in the trunk may cause an electrical short in the signal acquisition module, increasing the risk of fire or crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V677000·2022-09-12

    Farber Recalls One 2021 Freightliner XC Due to Lighting Failure Risk

    Farber Specialty Vehicles is recalling one 2021 Freightliner XC because an incorrectly installed resistor can cause vehicle lighting to fail, increasing crash risk.

    Product
    FARBER SPECIALTY — FARBER SPECIALTY FCCC XC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V680000·2022-09-12

    Mercedes-Benz Recalls GLE and GLS Models for Rear Window Trim Defect

    Mercedes-Benz is recalling certain 2020-2022 GLE and GLS models because rear door window trim bars may detach, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 400 E, GLE 350, GLE 450, GLS 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-09102022-01·2022-09-10

    USDA Issues Public Health Alert for HelloFresh Ground Beef Due to E. Coli Risk

    USDA FSIS issued a public health alert for specific HelloFresh ground beef packages linked to an E. coli O157:H7 outbreak. Consumers are urged to discard the product.

    Product
    FSIS Issues Public Health Alert For Specific Ground Beef In HelloFresh Meal Kits Due to Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·22771·2022-09-08

    Murphy Beds Recalled Due to Serious Impact and Crush Hazards

    Murphy beds sold under Ivy Bronx, Orren Ellis, Stellar Home Furniture, and Wade Logan brand names can break or detach from walls and fall, posing crush and impact hazards. The manufacturer has received 146 reports of failures with 62 injuries.

    Product
    Ivy Bronx, Orren Ellis, Stellar Home Furniture, and Wade Logan branded Murphy Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V675000·2022-09-08

    Ford Recalls 2022 F-150 Raptors Due to Wheel Lug Nut Tightening Issue

    Ford is recalling 2022 F-150 Raptor Series vehicles with 37-inch tires because incorrectly tightened wheel lug nuts may loosen, increasing the risk of wheel separation and a crash.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V672000·2022-09-08

    BMW Recalls 2022 CE 04 Motorcycles for Horn Attachment Defect

    BMW is recalling 2022 CE 04 motorcycles because the horn may loosen or detach, potentially interfering with steering and increasing crash risk.

    Product
    BMW — BMW CE 04
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V673000·2022-09-08

    2022 Audi Q3 Fuel Tank Vent Pipe May Leak Gasoline

    Audi is recalling certain 2022 and 2021 Q3 vehicles due to a damaged vent pipe in the fuel tank that may allow gasoline to spill when the fuel cap is opened, increasing the risk of injury.

    Product
    AUDI — AUDI Q3
    Category
    Vehicle
    Distribution
    Distributed nationwide