The Recall Desk

State

Oregon product recalls

72,966 recalls have nationwide distribution and so reach Oregon. 7,526 additional recalls listed Oregon specifically in their distribution scope.

What the numbers show

Total
7,526
Critical
876
Severe
1,803
Most recent
2026-09-16

Of the 7,525 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 1,803 (24%) are Severe. The remaining 1 are awaiting that pass and carry the agency’s own text in the meantime; they are not counted above, because scoring them before reading them would be a guess.

These figures cover only the 7,526 recalls whose distribution notice names Oregon specifically. The 72,966 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5601–5625 of 80492

  • ModerateFDA (Devices)·Z-2493-2025·2025-09-10

    RayStation 12A planning software recalled over duplicate DICOM instance identifier risk

    RayStation 12A and its service packs are recalled because DICOM instance identifiers from the RayGateway interface to Accuray's iDMS are not guaranteed to be unique.

    Product
    RayStation with the following product descriptions: 1. RayStation 12A, Software Version: 13.0.0.1547. 2. RayStation 12A Service Pack 1, Software Version: 13.1.0.144. 3. RayStation 12A Service Pack 2, Software Version: 13.1.1.89. Product Description: Radiation Thera
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2497-2025·2025-09-10

    LIFEPAK 15 defibrillators recalled because post-service inspections were not performed

    Four LIFEPAK 15 defibrillators are recalled because required inspections were not performed on units that had gone through servicing.

    Product
    LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 / 99577-001957 / 883873871690 V15-2-000051 / 99577-000046 / 883873988022 V15-2-000099 / 99577-000093 / 883873979020 V15-2-001603 / 99577-001256 / 883873911631 LIFEPAK 15: The LP15 is intended for use by trained
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2518-2025·2025-09-10

    Hemodynamic recording systems recalled over pressure sensor error during blood pressure measurement

    Merge Hemo systems are recalled because certain Schiller ARGUS PB-3000 patient data modules trigger a Pressure Sensor Defective error during non-invasive blood pressure measurement above 240 mmHg. 84 units are affected.

    Product
    Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Product Description: The Merge Hemo, Model RCSV2 device is a hemodynamics recording computer system that monitors, measures, displays, records and stores various physiologic and blood fl
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2489-2025·2025-09-10

    RayStation 9B and 10A software recalled over non-unique DICOM identifiers

    RayStation 9B, 9B SP1, 10A and 10A service pack radiation therapy planning software is recalled because DICOM instance identifiers from the RayGateway interface are not guaranteed to be unique.

    Product
    RayStation with the following product descriptions: 1. RayStation 9B, Software Version: 9.1.0.933. 2. RayStation 9B Service Pack 1, Software Version: 9.2.0.483. 3. RayStation 10A, Software Version: 10.0.0.1154. 4. RayStation 10A Service Pack 1, Software Version: 10.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2516-2025·2025-09-10

    Spinal implant inserters recalled over potential missing pins at the tip

    TOPS Inserters, model 82889, part of the TOPS System Instrument Set, are recalled because of the potential for missing pins at the tip of the inserter. 30 units are affected.

    Product
    TOPS Inserter, part of the TOPS System Instrument Set used for implantation of the TOPS System. Model Number: 82889.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2504-2025·2025-09-10

    Fluoroscopic X-ray systems recalled over air baffle missing from internal PCs

    Philips Allura Xper interventional fluoroscopic X-ray systems are recalled because an air baffle component may be missing in some Nehalem FlexVision-2 PCs. 192 units are affected.

    Product
    Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series. Labeled as the following with corresponding model numbers: 1. Allura Xper FD10, Model Number 722003. 2. Allura Xper FD10/10, Model Number 722005. 3. Allura Xper FD20, Model Number 722006. 4. All
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0615-2025·2025-09-10

    Sulfamethoxazole and trimethoprim tablets recalled over micro-organism on packaging coil

    Amneal sulfamethoxazole and trimethoprim double strength tablets are recalled because a micro-organism was detected on a lot of auxiliary polyester coil used in packaging. No micro-organism was found on any tablets.

    Product
    SULFAMETHOXAZOLE AND TRIMETHOPRIM — SULFAMETHOXAZOLE AND TRIMETHOPRIM (SULFAMETHOXAZOLE AND TRIMETHOPRIM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2495-2025·2025-09-10

    RayStation 2023B and 2024A software recalled over non-unique DICOM identifiers

    RayStation 2023B, 2024A and 2024A SP3 radiation therapy planning software is recalled because DICOM instance identifiers from the RayGateway interface are not guaranteed to be unique.

    Product
    RayStation with the following product descriptions: 1. RayStation 2023B, Software Version: 14.0.0.3338. 2. RayStation 2024A, Software Version: 15.0.0.430. 3. RayStation 2024A SP3, Software Version: 15.1.3.10. Product Description: Radiation Therapy Treatment Plannin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2491-2025·2025-09-10

    RayStation 11A planning software recalled over non-unique DICOM instance identifiers

    RayStation 11A and its service packs are recalled because DICOM instance identifiers from the RayGateway interface to Accuray's iDMS are not guaranteed to be unique.

    Product
    RayStation with the following product descriptions: 1. RayStation 11A, Software Version: 11.0.0.951. 2. RayStation 11A Service Pack 1, Software Version: 11.0.1.29. 3. RayStation 11A Service Pack 2, Software Version: 11.0.3.116. 4. RayStation 11A Service Pack 3, Softw
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0618-2025·2025-09-10

    Chlorpromazine 100 mg tablets recalled over micro-organism on packaging coil

    Amneal chlorpromazine hydrochloride tablets, 100 mg, are recalled because a micro-organism was detected on a lot of auxiliary polyester coil used in packaging. No micro-organism was found on any tablets.

    Product
    CHLORPROMAZINE HYDROCHLORIDE — CHLORPROMAZINE HYDROCHLORIDE (CHLORPROMAZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2517-2025·2025-09-10

    Flowmeter patches recalled over expiry date printed one year too early

    FloPatch FP120 flowmeter patches, lot 03250602, are recalled because the human readable expiry date on the outer shipping packaging reads 2025-06-20 when it should read 2026-06-20. 9 units are affected.

    Product
    FloPatch FP120, REF: FP120-FOT01-005
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V588000·2025-09-09

    Storyteller Overland Recalls GXV Hilt Vehicles for Wiring Fire Risk

    Storyteller Overland is recalling 2024-2026 GXV Hilt recreational vehicles because auxiliary power system wires may be damaged, increasing the risk of a fire.

    Product
    STORYTELLER OVERLAND — STORYTELLER OVERLAND GXV HILT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V586000·2025-09-09

    Alfa Romeo Giulia and Stelvio Recalled for Fuel Pump Failure Risk

    Chrysler is recalling 2017-2019 Alfa Romeo Giulia and 2018-2019 Stelvio vehicles because a failing fuel pump may cause loss of drive power, increasing crash risk.

    Product
    ALFA ROMEO — ALFA ROMEO GIULIA, STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V587000·2025-09-09

    Zero Motorcycles Recalls 2023-2024 Models Due to Wiring Defect

    Zero Motorcycles is recalling 2023-2024 DSR, DSR/X, DS, and DSRP models because improperly routed wires may break, causing a loss of drive power and increasing crash risk.

    Product
    ZERO — ZERO DS, DSR, DSR/X, DSRP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V585000·2025-09-08

    2025 Rivian R1S and R1T Recalled Due to Software Defect

    Rivian is recalling certain 2025 R1S and R1T vehicles because the Hands-Free Highway Assist software may fail to detect lead vehicles, increasing crash risk. A free over-the-air software update is available.

    Product
    RIVIAN — RIVIAN R1S, R1T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V584000·2025-09-06

    Spartan Fire Recalls Fire Trucks Due to Door Latch Defect

    Spartan Fire is recalling specific 2023-2026 fire trucks because a door latch defect may prevent the cab door from opening, potentially trapping occupants.

    Product
    SPARTAN FIRE — SPARTAN FIRE, KME METROSTAR, redundant PREDATOR, PREDATOR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V582000·2025-09-05

    2025 Acura RDX Electric Power Steering Software Calibration Defect

    Honda is recalling certain 2025 Acura RDX vehicles because the electric power steering software may not be properly calibrated, which can cause loss of power steering assist and increase crash risk.

    Product
    ACURA — ACURA RDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V583000·2025-09-05

    Honda CRF1100 Africa Twin Motorcycles Handlebar Switch Corrosion

    Honda is recalling certain 2020–2025 CRF1100 Africa Twin motorcycles due to corrosion of the left handlebar switch harness, which may disable the horn or headlight beam-switching function. This electrical failure increases crash and injury risk.

    Product
    HONDA — HONDA CRF1100
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V574000·2025-09-04

    2025 Jeep Wagoneer S Incorrectly Installed Spring Disables Park Function

    Chrysler recalls 2024-2025 Jeep Wagoneer S and Dodge Charger electric vehicles due to an incorrectly installed spring that may disable the park function, potentially causing vehicle rollaway.

    Product
    DODGE — DODGE, JEEP CHARGER EV, WAGONEER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25455·2025-09-04

    Cordless grease guns recalled after hose failures caused five laceration injuries

    About 62,927 Makita professional cordless grease guns and grease gun hoses are recalled because the flexible hose can develop a hole and eject grease. Five hose failures with laceration injuries were reported.

    Product
    Makita Professional Cordless Grease Guns and Makita Grease Gun Hoses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V575000·2025-09-04

    2025 Jeep Wagoneer S Recalled for Incorrect Cross Beam

    Chrysler is recalling certain 2025 Jeep Wagoneer S vehicles with an incorrect cross car beam in the instrument panel. The defect may not adequately protect occupants in a crash.

    Product
    JEEP — JEEP WAGONEER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V573000·2025-09-04

    2025 Chrysler Pacifica side curtain air bags recalled for inadequate pressure retention

    Chrysler is recalling certain 2025 Pacifica and Voyager vehicles due to defective side curtain air bags. The air bags may have insufficient pressure retention from improperly sealed seams, increasing the risk of ejection during a crash.

    Product
    CHRYSLER — CHRYSLER PACIFICA, VOYAGER
    Category
    Vehicle
    Distribution
    Distributed nationwide