The Recall Desk

State

Oregon product recalls

73,486 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 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23726–23750 of 81019

  • ModerateFDA (Drugs)·D-0500-2022·2022-02-09

    Magnacal Calcium Carbonate Tablets Recalled for cGMP Deviations

    Ultra Seal Corporation is recalling MAGNACAL calcium carbonate 420 mg tablets (Lot #AK9768, expiration 08/2022) nationwide due to current Good Manufacturing Practice (cGMP) deviations. The voluntary recall was initiated on January 24, 2022.

    Product
    MAGNACAL (calcium carbonate 420 mg), 2 tablet packets, Manufactured for: Afassco Inc. Minden, NV 89423
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0522-2022·2022-02-09

    Prescription Drug Recall: Mimvey Mislabeling by Teva Pharmaceuticals

    Teva Pharmaceuticals USA is recalling Mimvey (estradiol and norethindrone acetate) tablets nationwide due to mislabeling. The recall affects 6,430 cartons distributed throughout the USA.

    Product
    MIMVEY — MIMVEY (ESTRADIOL AND NORETHINDRONE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0521-2022·2022-02-09

    Mimvey Estradiol/Norethindrone Prescription Drug Mislabeling Recall

    Teva Pharmaceuticals USA is recalling Mimvey (estradiol and norethindrone acetate) tablets nationwide due to mislabeling on certain cartons. The recall affects 218,174 cartons distributed in the United States.

    Product
    MIMVEY — MIMVEY (ESTRADIOL AND NORETHINDRONE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V068000·2022-02-08

    Tiffin motorhomes have improperly secured buss bars increasing fire risk

    Tiffin is recalling 2018-2022 Allegro and Allegro Breeze motorhomes where an improperly secured electrical buss bar can cause the DC Distribution Panel to overheat and potentially start fires. Dealers will replace the buss bar with a cable for free.

    Product
    TIFFIN — TIFFIN ALLEGRO, ALLEGRO BREEZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V067000·2022-02-08

    Holiday House Travel Trailers Propane Regulator Failure Risk

    Holiday House is recalling certain 2019–2021 travel trailers equipped with defective Winntec propane regulators that may fail and increase propane pressure, raising fire risk in gas appliances.

    Product
    HOLIDAY HOUSE — HOLIDAY HOUSE 24TB, 27RQ, 18RB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V065000·2022-02-07

    Roadtrek Recreational Vehicles Recalled for Unattached Propane Lines

    Roadtrek is recalling certain 2021-2022 recreational vehicles because the propane line may not be attached to the water heater. An unattached propane line can allow gas to enter the vehicle, increasing the risk of a fire.

    Product
    ROADTREK — ROADTREK ZION SRT, ZION SLUMBER, ZION, PLAY SLUMBER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V064000·2022-02-07

    Audi Recalls 2022 Q3 Vehicles for Rearview Camera Software Error

    Audi is recalling 2022 Q3 vehicles because a software error may prevent the rearview camera from displaying an image when reversing, increasing crash risk.

    Product
    AUDI — AUDI Q3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V063000·2022-02-04

    Tesla Model Y Boombox Feature May Obscure Pedestrian Warning System

    Tesla is recalling certain 2020-2022 Model Y vehicles because the Boombox feature can obscure the Pedestrian Warning System sounds, creating a collision risk. Tesla will disable the Boombox in Drive, Neutral, and Reverse modes via software update.

    Product
    TESLA — TESLA MODEL 3, MODEL X, MODEL Y, MODEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V056000·2022-02-03

    Hyundai Recalls Vehicles Due to ABS Module Fire Risk

    Hyundai is recalling specific 2014-2019 models because a faulty ABS module could cause an electrical short and engine compartment fire.

    Product
    HYUNDAI — HYUNDAI TUCSON, SANTA FE, SANTA FE SPORT, SANTA FE XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V061000·2022-02-03

    Honda Recalls 2021 CBR1000RR-R Fireblade SP Motorcycles for Fire Risk

    Honda is recalling 2021 CBR1000RR-R Fireblade SP motorcycles because an overheating exhaust pipe could melt the oil cooler pipe, causing a leak that increases the risk of fire or crash.

    Product
    HONDA — HONDA CBR1000RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E006000·2022-02-03

    Nexxpro Recalls X.R2 Motorcycle Helmets Due to Impact Protection Defect

    Nexxpro is recalling specific X.R2 motorcycle helmets because they may not adequately protect the wearer in a crash. Owners will receive free replacements.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V058000·2022-02-03

    Altec Recalls 2017-2021 LS60 Aerial Devices Due to Bearing Bolt Risk

    Altec is recalling 2017-2021 LS60 aerial devices because bearing bolt washers may interfere with welds, causing bolts to break and increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V059000·2022-02-03

    Class C Motorhomes Recalled for Defective Steering Bolts

    Jayco is recalling certain 2021-2022 Entegra Coach Accolade and Jayco Seneca Class C motorhomes because steering arm and tie rod bolts may fracture, causing loss of steering control. Free replacement available.

    Product
    ENTEGRA — ENTEGRA, JAYCO ACCOLADE XL, SENECA PRESTIGE, SENECA, ACCOLADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22719·2022-02-03

    River Street Five-Drawer Chests Recalled for Tip-Over and Entrapment Hazards

    BFG North Carolina is recalling about 1,380 River Street Five-Drawer Chests sold at Rooms To Go from February 2019 through October 2021. The dressers are unstable if not anchored to the wall, posing tip-over and entrapment hazards that may result in death or serious injuries to children.

    Product
    River Street Five-Drawer Chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V057000·2022-02-03

    Highland Ridge RV Recalls 2022 Olympia Models Due to Electrical Grounding Defect

    Highland Ridge RV is recalling 2022 Olympia and Olympia Sport recreational vehicles because the metallic electrical box may not be grounded, posing a risk of electric shock.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT OLYMPIA, OLYMPIA SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V053000·2022-02-02

    2021-2022 Jayco and Entegra motorhomes recalled for loose tie rod clamps

    Jayco and Entegra are recalling certain 2021-2022 Class C motorhomes with loose tie rod clamps that could lead to steering loss and increased crash risk.

    Product
    JAYCO — JAYCO, ENTEGRA SENECA, ACCOLADE, ACCOLADE XL, SENECA PRESTIGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0398-2022·2022-02-02

    Cefuroxime Sterile Ophthalmic Injection Recalled Due to Sterility Concerns

    Edge Pharma is recalling Cefuroxime sterile ophthalmic solution for injection because the company cannot assure the product meets sterility requirements. The recall affects approximately 1,720 syringes distributed nationwide.

    Product
    Cefuroxime, Sterile Ophthalmic Solution for Injection, Preservative Free, 3mg/0.3mL (10 mg/mL), 0.3 mL single use syringe for Intraocular Injection, Edge Pharma, LLC, 656 Hercules Dr., Colchester, VT 05446 NDC 05446-1003-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0399-2022·2022-02-02

    Dexamethasone Sodium Phosphate Otic Injection Syringes Recalled for Lack of Sterility Assurance

    Edge Pharma LLC is recalling Dexamethasone sodium phosphate sterile otic solution for injection syringes (NDC 05446-0848-01) due to lack of assurance of sterility. Approximately 323 syringes were distributed nationwide.

    Product
    Dexamethasone sodium phosphate, sterile otic solution for injection Preservative free, 19.2 mg/0.8mL (24mg/mL), 0.8 mL per syringe Single Use Syringe For Otic Injection, Edge Pharma LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-0848-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0418-2022·2022-02-02

    Phenylephrine Injection Recall Due to Sterility Assurance Concerns

    Edge Pharma is recalling phenylephrine injection (20 mg/250 mL) because the manufacturer cannot assure the product maintains sterility. The recall affects 3,930 bags distributed nationwide.

    Product
    PHENYLephrine, 0.9% Sodium Chloride Injection, USP, 20 mg/250mL, (0.08 mg/mL), Single use bag for IV injection (Preservative Free), Rx Only, Edge Pharma, LLC, 856 Hercules Dr, Colchester, VT NDC 05446-1667-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0394-2022·2022-02-02

    ALUM Concentrate IV Bags Recalled for Lack of Sterility Assurance

    Edge Pharma, LLC is recalling ALUM Concentrate (Aluminum Potassium Sulfate Dodecahydrate) IV bags nationwide due to lack of assurance of sterility. The affected product is a prescription intravenous medication supplied in 300 ml bags.

    Product
    ALUM Concentrate (Aluminum Potassium Sulfate Dodecahydrate in Sterile Water (PF) 30 g/300 ml, IV bag, Rx Only, Edge Pharma, LLC, 856 Hercules Dr, Colchester, VT 05446, NDC 05446-0637-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0395-2022·2022-02-02

    Lidocaine HCl Sterile Buffered Solution Recalled for Lack of Sterility Assurance

    Edge Pharma is recalling Lidocaine HCl Sterile Buffered Solution for Injection (1%, 10 mL syringes) due to lack of assurance of sterility. The recall affects approximately 4,465 syringes distributed nationwide.

    Product
    Lidocaine HCl Sterile Buffered Solution for Injection (PF) 1%, 10mL per syringe, Single Use Syringe for Infiltration and Nerve Block, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-0850-10
    Category
    Drug
    Distribution
    Distributed nationwide