The Recall Desk

State

Oregon product recalls

73,388 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 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22751–22775 of 80919

  • HighNHTSA·22V215000·2022-04-01

    Mercedes-Maybach S 580 Recalled for Front Seat Trim Detachment Risk

    Mercedes-Benz is recalling 2021-2022 Maybach S 580 vehicles because front seat trim parts may detach during rear air bag deployment, potentially causing improper air bag function and injury.

    Product
    MERCEDES-MAYBACH — MERCEDES-MAYBACH S 580, S 580 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E029000·2022-03-31

    GM Recalls Truck Hero Tonneau Covers for Detachment Risk

    General Motors is recalling specific Truck Hero tonneau covers for 2019-2022 Chevrolet and GMC trucks because they may detach while driving, creating a road hazard.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V210000·2022-03-31

    Chevrolet Traverse roof rail air bag harness connector defect

    General Motors is recalling certain 2020-2022 Chevrolet Traverse and 2021-2022 Buick Enclave vehicles because the harness connector to the roof rail air bags may have incompatible electrical terminals that could prevent air bag deployment in a crash.

    Product
    CHEVROLET — CHEVROLET, BUICK TRAVERSE, ENCLAVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V212000·2022-03-31

    Jayco Recalls 2022 White Hawk Travel Trailers Due to Fire Risk

    Jayco is recalling 2022 White Hawk travel trailers because loose power inlet wiring may cause an electrical arc or short, increasing the risk of a fire.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER WHITE HAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22737·2022-03-31

    SOUNDBOKS Gen. 3 Bluetooth Speakers Recalled for Battery Fire Hazard

    SOUNDBOKS Inc. is recalling about 6,700 Gen. 3 Bluetooth speakers because the removable lithium-ion battery can overheat and pose a fire hazard. Consumers should stop using the speakers immediately and contact the company for a free replacement battery.

    Product
    SOUNDBOKS (Gen. 3) Bluetooth Speakers with Lithium-Ion Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V208000·2022-03-31

    2022 Keystone Alpine Travel Trailers Recalled for Electrical Fire Risk

    Keystone is recalling 2022 Alpine and related travel trailers due to power inlet lug bolts manufactured too hard to tighten properly, causing loose electrical connections that could lead to fire.

    Product
    KEYSTONE — KEYSTONE ALPINE, AVALANCHE, PASSPORT, IMPACT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22109·2022-03-31

    Helix Metal Lockable Drug Chests Recalled Due to Locking Mechanism Failure

    Maped Helix USA is recalling about 7,700 Helix Metal Lockable Drug Chests because the locking mechanism can fail, allowing unauthorized access to medications and posing a risk of poisoning.

    Product
    Helix Metal Lockable Drug Chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V209000·2022-03-31

    Keystone Cougar travel trailers recalled for outrigger tire clearance defect

    Keystone is recalling 2019-2022 Cougar travel trailers due to improper outrigger clearance that may allow tires to contact the outrigger. Damaged tires can fail and cause loss of vehicle control and increased crash risk.

    Product
    KEYSTONE — KEYSTONE COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22110·2022-03-31

    PlayMonster Kid O Hudson Glow Rattles Recalled for Choking Hazard

    PlayMonster is recalling Kid O Hudson Glow Rattles because the rattle's legs can break off, posing a choking hazard to young children. The firm has received three reports of legs breaking off, though no injuries have been reported.

    Product
    Kid O Hudson® Glow Rattles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22111·2022-03-31

    Universal Security Instruments 2-in-1 Smoke and Carbon Monoxide Alarms Recalled for Failure to Alert

    Universal Security Instruments is recalling about 8,000 combination smoke and carbon monoxide alarms that may fail to alert consumers to dangerous carbon monoxide levels. Two units have been reported to fail the alarm function, though no injuries have been reported.

    Product
    2-in-1 Photoelectric Smoke & Fire + Carbon Monoxide Alarms
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V207000·2022-03-31

    2022 Triumph Speed Triple RS Motorcycle Rear Brake Disc Bolts May Loosen

    Triumph is recalling 2022 Speed Triple RS and Speed Triple RR motorcycles because rear brake disc bolts may loosen, potentially preventing the wheel from rotating freely and increasing crash risk.

    Product
    TRIUMPH — TRIUMPH SPEED TRIPLE RS, SPEED TRIPLE RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0668-2022·2022-03-30

    Blaine Labs Revitaderm Wound Care Gel Recalled for Bacillus Contamination

    The FDA has recalled Revitaderm Wound Care gel (Benzalkonium Chloride 0.1%) distributed nationwide due to contamination with Bacillus cereus. The affected product was distributed to 45 doctors in 17 states.

    Product
    REVITADERM WOUND CARE — REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0785-2022·2022-03-30

    Philips Respironics respiratory ventilators recalled for foam degradation

    Philips Respironics recalls 229,353 respiratory ventilators because polyester-polyurethane foam may degrade and release particles. Foam degradation could compromise ventilator function.

    Product
    Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators The device is intended to be used in home, institution/hospital, and portable applications such as wheelchairs and gurneys, and may be used for both invasive and non-invasive ventilation. It is not…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0750-2022·2022-03-30

    Fresenius Kabi Sodium Acetate Injection Recalled for Particulate Matter

    Fresenius Kabi USA is recalling sodium acetate injection due to the presence of particulate matter composed of carbon, oxygen, iron, and trace elements in multiple lots distributed nationwide.

    Product
    SODIUM ACETATE — SODIUM ACETATE (SODIUM ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V205000·2022-03-30

    Daimler Recalls 2023 Western Star 4900 Trucks for Brake Line Defect

    Daimler Trucks North America is recalling 2023 Western Star 4900 trucks because incorrectly installed air lines may reduce brake performance, increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0724-2022·2022-03-30

    Sincalide Injection Recalled for Potency and Reconstitution Issues

    Olympia Compounding Pharmacy is recalling Sincalide lyophilized powder for injection due to concerns about super potency and failed reconstitution time. The product is distributed nationwide, including Puerto Rico.

    Product
    Sincalide Lyophilized powder for reconstitution Each ML contains: Mannitol 170mg, Arginine 30mg, Lysine 15mg, Potassium Phosphate 9mg, Methionine 4mg, Edetate Disodium Dihydrate 2mg, Polysorbate mcg, Water for Injection, Multiple Dose Injection 5 mcg Vial, Rx Only, Olympia…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0823-2022·2022-03-30

    NuOss Collagen Blocks Recalled Due to Product Substitution Error

    Ace Surgical Supply is recalling NuOss Collagen Blocks because some units were mistakenly packaged with Collatene Fibrillar Collagen instead, which may result in suboptimal bone repair during dental and maxillofacial procedures.

    Product
    NuOss Collagen Block Size 8mm x 9mm x 9mm- used in filling periodontal and maxillofacial defects. Catalog Number: 5099250
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0902-2022·2022-03-30

    PB Choc Protein Bites Recalled for Undeclared Coconut Allergen

    HumbleHungryHappy LLC is recalling PB Choc Protein Bites because coconut is not listed in the allergen declaration, posing a risk to consumers with coconut allergies.

    Product
    PB CHOC PROTEIN BITES, net wt. 7.2 oz. There are 6 bites in a rectangular flexible plastic clamshell covered with plastic film lid. Product label is read in parts: "***PB CHOC PROTEIN BITE***Ingredients: Peanut Butter, Coconut Milk, Orgain Organic Protein, Hershey Semi-Sweet…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0821-2022·2022-03-30

    Medical Device Air Supply Unit Recalled for Potential Electrical Shock Hazard

    Baxter Healthcare is recalling the Compella Therapy Air Supply Unit due to potential power cord damage that could expose electrical conductors and create a shock risk. The recall affects 6,022 units distributed worldwide.

    Product
    Compella Therapy Air Supply Unit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V206000·2022-03-30

    2022 Keystone Passport Travel Trailers Recalled for Incorrect Axles and Tires

    Keystone RV Company is recalling 2022 Passport travel trailers equipped with incorrect size axles and tires that could cause overloading. Dealers will replace the suspension components free of charge.

    Product
    KEYSTONE — KEYSTONE PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0717-2022·2022-03-30

    Eye Lubricant Drops Recalled for Insufficient Sterility Assurance

    Akorn, Inc. is recalling 62,331 boxes of TheraTears Extra lubricant eye drops distributed nationwide due to lack of assured sterility. Non-sterile eye drops could pose infection risks.

    Product
    THERATEARS EXTRA — THERATEARS EXTRA (CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0683-2022·2022-03-30

    Fluocinonide Cream Recalled for Manufacturing Compliance and Stability Deviations

    Teligent Pharma, Inc. is recalling Fluocinonide Cream USP 0.1% due to manufacturing compliance deviations and discontinuation of stability studies. The recall affects products nationwide in the USA and Puerto Rico.

    Product
    Fluocinonide Cream USP, 0.1%, 120 grams tube, Rx Only, Manufactured by: Teligent Pharma, Inc., Buena, New Jersey 08310, NDC 52565-079-11.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0719-2022·2022-03-30

    FDA Recalls NAD+ Injection Due to Sub-Potency and Stability Concerns

    Olympia Compounding Pharmacy is recalling NAD+ Nicotinamide Adenine Dinucleotide injection vials nationwide due to sub-potency or exceeded reconstitution time.

    Product
    NAD+ Nicotinamide Adenine Dinucleotide, Lyophilized powder for reconstitution, Multi-Dose 500 mg per vial, Each ML contains: 0.288% Sodium Phosphate Monobasic USP, 0.42% Sodium Phosphate Dibasic USP, 5% Mannitol USP, Sterile Water for Injection USP, Rx Only, Olympia…
    Category
    Drug
    Distribution
    Distributed nationwide