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.

21151–21175 of 80919

  • ModerateFDA (Devices)·Z-1386-2022·2022-07-27

    Stryker Trevo Trak 21 Microcatheter recalled for missing carton product illustration

    Stryker Neurovascular is recalling 71 Trevo Trak 21 Microcatheter units because the product carton label is missing the required product drawing or illustration.

    Product
    Trevo Trak 21 Microcatheter, REF: 90338. TREVO NXT 3X32+TRAK21 2-PACK - CE, REF: 91412; TREVO NXT 4X28+TRAK21 2-PACK - CE, REF: 91413; TREVO NXT 4X41+TRAK21 2-PACK - CE, REF: 91414; TREVO NXT 6X37+TRAK21 2-PACK - CE, REF: 91415; TREVO NXT 4X28+TRAK21+CAT6 3-PACK - CE…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1422-2022·2022-07-27

    Laboratory Reagent Recalled Due to Inaccurate Calibration Curves

    Randox Laboratories is recalling Soluble Transferrin Receptor reagent (TF10159) due to calibration curve defects causing inaccurate test results on Siemens Atellica CH analyzers.

    Product
    Soluble Transferrin Receptors (STFR), Catalog Number TF10159 (Research Use Only). IVD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1423-2022·2022-07-27

    Soluble Transferrin Receptor Calibrator Recall Due to Lab Errors

    Randox Laboratories is recalling Soluble Transferrin Receptors Calibrator kits used in lab analyzers. The calibrators can produce incorrect test results, with some values potentially underestimated by up to 30 percent.

    Product
    Soluble Transferrin Receptors Calibrator Series (STFR CAL), Catalog Number TF10161. IVD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1340-2022·2022-07-27

    FDA Recalls Launch Sequence Euphoria Capsules as Unapproved Drug

    Launch Sequence Euphoria Capsules were marketed without FDA approval. Consumers should discontinue use immediately and contact the manufacturer.

    Product
    Launch Sequence Euphoria Capsules, 10- count tins, ASIN B08ZJX4V9J, UPC Code 661020846864.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1244-2022·2022-07-27

    OTC Hydrogen Peroxide Solution Recalled for Isopropyl Alcohol Contamination

    Vi-Jon's hydrogen peroxide topical solution has been recalled due to cross-contamination with low levels of isopropyl alcohol. Multiple brands are affected nationwide in the USA and Canada.

    Product
    HYDROGEN PEROXIDE — HYDROGEN PEROXIDE (HYDROGEN PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1394-2022·2022-07-27

    Triton Sponge System Software Instructions Updated for Proper Sponge Handling

    Stryker is updating the Instructions for Use for the Triton Sponge System software (versions 4.6.5, 4.8.7, 4.9.6) to clarify proper handling technique for sponges and calibration placard. The FDA Class III recall affects 51 units distributed nationwide.

    Product
    Triton Sponge System (Software), GAUS-3, Software Versions 4.6.5, 4.8.7, 4.9.6
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1390-2022·2022-07-27

    Erythropoietin Control Product Instructions Contain Incorrect CE Marking

    R & D Systems is replacing Instructions for Use (IFU) for Quantikine IVD Erythropoietin Human Serum Controls due to an incorrect CE marking designation that should not appear on the self-certified product.

    Product
    Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative controls for the determination of Erythropoietin concentrations in human serum and plasma. IFU, Part Number 750095
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1393-2022·2022-07-27

    NeuRx Diaphragm Pacing System Labeling Revised for Storage Clarity

    Synapse Biomedical revised labeling for the NeuRx Diaphragm Pacing System to clarify that temperature range symbols indicate storage conditions, not transport or package conditions. The revision affects 71 units distributed in the United States.

    Product
    NeuRx Diaphragm Pacing System (NeuRx DPS), Affected part numbers: Part # Part Name 20-0035 NeuRx DPS System Kit 20-0036 NeuRx Diaphragm Pacing System, Patient Kit, SCI 20-0028 NeuRx DPS Surgical Kit, HDE 20-0040 NeuRx Diaphragm Pacing…
    Category
    Medical Device
    Distribution
    19 states
  • SevereNHTSA·22V539000·2022-07-26

    Spartan Fire Recalls 2020-2021 Metrostar and Gladiator Trucks for Fire Risk

    Spartan Fire is recalling 2020-2021 Metrostar and Gladiator fire trucks because a loose electrical connection may cause the load center to overheat and increase the risk of a fire.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V537000·2022-07-26

    Capacity Recalls 2021-2022 TJ Trucks for Steering Gear Fracture Risk

    Capacity of Texas is recalling 2021-2022 TJ 5000, 6500, and 9000 trucks because incorrectly assembled steering gears may fracture, causing loss of steering control.

    Product
    CAPACITY — CAPACITY TJ 9000, TJ 6500, TJ 5000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V538000·2022-07-26

    E-One Fire Trucks Recalled for Electrical Connection Overheating Risk

    E-One is recalling specific 2019-2022 fire trucks because a loose electrical connection may cause the load center to overheat, increasing fire risk.

    Product
    E-ONE — E-ONE CYCLONE II, TYPHOON, TYPHOON N, CYCLONE N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V536000·2022-07-26

    Ferrari Recalls Multiple Models Due to Brake Fluid Reservoir Cap Defect

    Ferrari is recalling various models from 2005-2022 because a defective brake fluid reservoir cap may cause a leak, leading to partial or total loss of brake function.

    Product
    FERRARI — FERRARI LAFERRARI, LAFERRARI APERTA, 612 SCAGLIETTI, F12 BERLINETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V529000·2022-07-22

    Ember Recalls 2022 Overland Trailers Due to LP Gas Leak Risk

    Ember is recalling 2022 Overland series trailers because cracked LP gas fittings may cause a leak, increasing the risk of fire.

    Product
    EMBER — EMBER OVERLAND SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V531000·2022-07-22

    Spartan RV Chassis Steering Gear Assembly Defect Recall

    Shyft Group is recalling certain 2022-2023 Spartan RV Chassis vehicles due to improperly assembled steering gears that may fracture, causing loss of steering control. Owners should contact the manufacturer for free inspection and replacement.

    Product
    SPARTAN — SPARTAN K3, K2, K4, K1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V528000·2022-07-22

    2022 Ford F-53 Steering Wheel Attachment Bolt May Loosen

    Ford is recalling certain 2022 F-53 and F-59 motorhome and commercial chassis vehicles because the steering wheel attachment bolt may loosen and separate. This could result in loss of steering control and increased crash risk.

    Product
    FORD — FORD F-59, F-53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V532000·2022-07-22

    Thomas Built Buses Minotour Recalled for Incorrect Tire Labeling

    Daimler Trucks North America is recalling 2019-2023 Thomas Built Buses Minotour school buses because tire labels list the wrong size, potentially affecting vehicle stability.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR SRW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V534000·2022-07-22

    Monroe Towmaster Recalls Trailers With Incorrect Tire Load Ratings

    Monroe Towmaster is recalling 2021-2022 TC-14D, T-24, and TC-24 trailers because installed tires have a lower load rating than required, increasing the risk of tire failure and crashes.

    Product
    TOWMASTER — TOWMASTER TC-14D, TC-24, T-24
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V533000·2022-07-22

    Mercedes-Benz AMG vehicles: transmission wiring fire hazard, 2019-2022

    Mercedes-Benz has recalled certain 2019–2022 AMG vehicles (CLS53, E53, GT53, and GT43 models) due to transmission wiring harness misrouting that can expose electrical connectors to corrosion, creating a fire risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT53, AMG E53, AMG CLS53, AMG GT43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V523000·2022-07-21

    2022 and 2023 Land Rover Defender seat belt pretensioner defect recall

    Jaguar Land Rover is recalling certain 2022-2023 Land Rover Defender and other models due to defective front seat belt pretensioners that may fail to properly restrain occupants in a crash, increasing injury risk.

    Product
    LAND ROVER — LAND ROVER DEFENDER, DISCOVERY, RANGE ROVER VELAR, DISCOVERY SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V519000·2022-07-21

    2022 Toyota RAV4 Air Bag Sensor May Deploy Incorrectly

    Toyota is recalling 2022 RAV4, RAV4 Hybrid, and RAV4 Prime vehicles because a front passenger seat occupant detection sensor may fail to properly detect occupants. This could cause improper air bag deployment during a crash, increasing injury risk.

    Product
    TOYOTA — TOYOTA RAV4 PRIME, RAV4 HYBRID, RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V524000·2022-07-21

    2022 Jaguar XF, F-Type, F-Pace seat belt pretensioner failure

    Jaguar is recalling 2022 XF, F-Type, and F-Pace vehicles because the driver and front passenger seat belt pretensioners may be damaged, causing improper restraint during a crash.

    Product
    JAGUAR — JAGUAR F-PACE, XF, F-TYPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22186·2022-07-21

    Key West Knock Down Hammock Stands Recalled for Fall Hazard

    The Hammock Source is recalling about 32,500 Key West Knock Down Hammock Stands because the weld attaching the stand to the base can break, posing a fall hazard. Nine reports of stands breaking have been received, including two reports of scrapes and bruises.

    Product
    Key West Knock Down Hammock Stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V527000·2022-07-21

    2022 Nissan Pathfinder rearview camera may fail due to software issue

    Nissan recalls 2022 Pathfinder rental vehicles where a software defect can disable the rearview camera, increasing crash risk. Affected customers will receive a free software update via dealer or over-the-air update.

    Product
    NISSAN — NISSAN TITAN, redundant ROGUE, FRONTIER, PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide