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.

24076–24100 of 81019

ModerateFDA (Drugs)·D-0364-2022·2022-01-19
The Natural Dentist Mouthwash Label Mix-Up Recall
The Natural Dentist Healthy Balance Peppermint Sage mouthwash (16.9 FL OZ, Lot 2091A) has been recalled due to a back label mix-up. The label incorrectly identifies the active ingredient as Menthol with the wrong UPC code instead of the correct Peppermint Oil and Sage Oil.
Product
The Natural Dentist Healthy Balance Peppermint Sage, Menthol 0.12%, 16.9 FL OZ (500 mL) bottles, Manufactured for Revive Personal Products Company, Madison, NJ 07940, UPC 7 14132 00071 4
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0365-2022·2022-01-19
Carbamazepine tablets recalled for failed dissolution specifications
Torrent Pharma Inc. is recalling Carbamazepine 200 mg tablets nationwide because they failed to meet dissolution specifications, which means the tablets may not release the medication properly in the body.
Product
CARBAMAZEPINE — CARBAMAZEPINE (CARBAMAZEPINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0482-2022·2022-01-19
Instavac Portable Suction Pumps Recalled for Premature Device Failures
Ohio Medical Corporation is recalling Instavac Portable Suction Pumps (models 757000, 756000, and replacement pump part #AI5511) due to an increase in premature device failures. Affected units were distributed nationwide.
Product
Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and Intermittent mode (model 756000, Instavac I); and Instavac replacement pumps, part #AI5511, a component of model numbers 756000 and 757000.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0368-2022·2022-01-19
Oxycodone Hydrochloride Oral Solution recalled for missing label
Akorn, Inc. is recalling Oxycodone Hydrochloride Oral Solution 5 mg per 5 mL distributed nationwide due to missing label.
Product
Oxycodone Hydrochloride Oral Solution, USP 5 mg per 5 mL (1 mg/mL), 500 mL bottle, Rx only, Manufactured by: Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701 --- NDC 50383-961-34
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0367-2022·2022-01-19
Morphine Sulfate Oral Solution 20 mg/mL recalled for missing label
Akorn, Inc. is recalling Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) in 30 mL bottles nationwide due to missing labeling on approximately 10,836 bottles.
Product
Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) 30 mL bottles, Rx only, Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701 -- NDC 50383-965-30
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V016000·2022-01-18
2022 Peterbilt 579 chassis step bolts may loosen and cause injury
Bolts securing the chassis fairing step assembly on certain 2022 Peterbilt 579 vehicles may loosen and fracture. This can cause the step to move unexpectedly while entering or exiting the cab, increasing the risk of injury.
Product
PETERBILT — PETERBILT 579
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V015000·2022-01-17
2022 Keystone Alpine RV Exterior Ladder May Detach from Rear Wall
Keystone RV Company is recalling certain 2022 Alpine and Avalanche vehicles due to improperly secured exterior ladders that may detach while in use, creating a risk of injury.
Product
KEYSTONE — KEYSTONE ALPINE, AVALANCHE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22E002000·2022-01-14
Tenneco Recalls Aftermarket Ball Joints for Toyota Sequoia and Tundra
Tenneco Automotive is recalling aftermarket ball joints for 2004-2007 Toyota Sequoia and 2004-2006 Toyota Tundra vehicles due to potential premature failure.
Product
TOYOTA — TOYOTA SEQUOIA, TUNDRA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V014000·2022-01-14
KTM Recalls 2022 Husqvarna Motorcycles for Brake Pad Retaining Clip Defect
KTM is recalling 2022 Husqvarna FE 350S and FE 501S motorcycles because incorrectly mounted front brake pad retaining clips may cause pads to detach, reducing braking performance.
Product
HUSQVARNA — HUSQVARNA FE 350S, FE 501S
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V013000·2022-01-14
2021 Ford Diesel Trucks Fuel Filter Cap Defect Fire Risk
Ford is recalling certain 2021 diesel trucks due to a void in the secondary fuel filter cap that may leak fuel, posing a fire risk. Dealers will replace the fuel filters free of charge.
Product
FORD — FORD F-550 SD, F-450 SD, F-650, F-250 SD
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V012000·2022-01-14
2022 Forest River Cherokee toy hauler tires may be incorrectly specified on placard
Forest River is recalling certain 2022 Cherokee toy haulers because the Tire and Loading Information placard may show incorrect rim specifications, potentially causing improper tire installation and crash risk.
Product
FOREST RIVER — FOREST RIVER CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22E001000·2022-01-13
Volta Power Systems Recalls Adaptor Harnesses Due to Fire Risk
Volta Power Systems is recalling 646 adaptor harnesses because incorrect construction may cause overheating and fire.
Product
ELECTRICAL SYSTEM:WIRING recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V011000·2022-01-13
Ford Recalls Fusion, MKZ, and Mustang for Brake Pedal Bumper Defect
Ford is recalling 2014-2015 Fusion, Lincoln MKZ, and 2015 Mustang vehicles because brake pedal bumpers may corrode and separate, potentially causing brake light confusion or rollaway risks.
Product
FORD — FORD, LINCOLN FUSION, MKZ, MUSTANG
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V010000·2022-01-13
Seagrave Recalls 2011-2021 Firetrucks Due to Cracking Crossmember Plate
Seagrave is recalling 2011-2021 Marauder and Capitol firetrucks because a crossmember mounting plate may crack, potentially distracting the driver and increasing crash risk.
Product
SEAGRAVE — SEAGRAVE MARAUDER, CAPITAL
Category
Vehicle
Distribution
Distributed nationwide
ModerateCPSC·22717·2022-01-13
Textron E-Z-GO Freedom RXV Personal Transportation Vehicles Recalled Due to Fall Hazards
Textron Specialized Vehicles is recalling about 280 E-Z-GO Freedom RXV personal transportation vehicles with rear-facing seats because the rear seat structure can fail and tilt unexpectedly, creating a fall and injury hazard. Consumers should stop using the rear-facing seat and contact Textron for a free repair.
Product
E-Z-GO Freedom RXV with Rear Facing Seat Personal Transportation Vehicles (PTV)
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0445-2022·2022-01-12
Power wheelchairs with LiNX Gyro module recalled for deceleration control failure
Invacare power wheelchairs with LiNX Gyro firmware 6.1.2 may decelerate more aggressively than programmed, risking user injury due to an incorrect deceleration profile.
Product
Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: TDX SP2: TDXSP2, TDXSP2-CG, TDXSP2X-CG, TDXSP2-MCG, TDXSP2X-MCG, TDXSP2V, TDXSP2V-HD, TDXSP2HD, TDXSP2HD-CG, TDXSP2HD-MCG
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22052·2022-01-12
EGL and ACE Youth All-Terrain Vehicles Recalled for Safety Standard Violations
EGL Motor is recalling about 2,900 EGL and ACE branded youth ATVs (models MADIX 125 and D110) because they fail federal safety standards, allowing children to exceed safe speeds and creating laceration and crash hazards.
Product
EGL and ACE Branded Youth All-Terrain Vehicles (ATVs)
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22053·2022-01-12
Children's Robes Recalled for Flammability Standards Violation
About 3,500 children's robes made by HulovoX fail federal flammability standards for sleepwear and pose a burn injury risk. The robes were sold online through Amazon.com from January to May 2021 for about $30 each.
Product
Children's Robes
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0461-2022·2022-01-12
Alinity m System Software Issue Affects Maintenance and Diagnostics Procedures
Abbott Molecular is recalling 742 Alinity m System units worldwide due to a software issue that prevents Field Service Engineers from properly completing maintenance and diagnostics procedures.
Product
Alinity m System, Part No. 08N53-002
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0449-2022·2022-01-12
Clinical Chemistry Analyzer Software Flaw May Cause Inaccurate Test Results
Siemens is recalling Atellica CH 930 clinical chemistry analyzers with software v1.25.1 or lower. Two software defects could cause inaccurate test results: test parameters may revert to defaults, or the analyzer may use expired reagents.
Product
Atellica CH 930 Analyzer with Software version: V1.25.1 and lower- An automated, clinical chemistry analyzer designed to perform in vitro diagnostic tests on clinical specimens. Siemens Material Number (SMN): 11067000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0446-2022·2022-01-12
Invacare AVIVA FX power wheelchair LiNX Gyro deceleration malfunction
Some Invacare AVIVA FX power wheelchairs with LiNX Gyro firmware 6.1.2 may decelerate more aggressively than programmed, creating injury risk.
Product
Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: IFX-20R, IFX-20SP, IFX-20MP, IFX-20C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0458-2022·2022-01-12
UROMEDICA Implantation Instrument Sheath May Damage ProACT Implants
Uromedica is recalling nonsterile implantation instrument sheaths (Lot UM00794 and UM00817) because the U-channel sheaths may damage ProACT implant devices during implantation procedures. Affected devices were distributed nationwide.
Product
UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar), REF 750041, nonsterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0448-2022·2022-01-12
Orthopedic Inserter Shaft Recalled for Mating Incompatibility During Surgery
Flower Orthopedics is recalling 48 units of the Flex-Thread Inserter Shaft due to mating incompatibility with the Inserter Draw Rod. The defect may cause the draw rod to bind during fibula intramedullary nail insertion, potentially preventing surgery completion.
Product
Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to be used with the Inserter Draw Rod and Blue Ratchet Handle in order to facilitate the insertion of the Flex-Thread Nail System- Catalog Number: 8435-1
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22051·2022-01-12
2021 Giant and Liv Adult Bicycles Recalled for Loose Handlebar Stem
Giant Bicycle Inc. is recalling about 20,800 units of 2021 Model Year Giant and Liv adult bicycles because the adjustable handlebar stem can become loose, posing fall and injury hazards. The company has received 86 reports of loose handlebars, including three reports of riders falling.
Product
2021 Model Year Giant and Liv Adult Bicycles
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0459-2022·2022-01-12
Surgical Instrument Tray Recalled for Incorrect Keel Punch Component
Howmedica Osteonics Corp. is recalling Triathlon Pro Tibial Preparation Trays that may contain the wrong surgical instrument. The incorrect component could delay surgery or cause unintended bone preparation during knee replacement procedures.
Product
Triathlon Pro Tibial Preparation Tray, Revision AC- for organization, storage, and transport in preparation for sterilization of re-usable instruments required for implanting the Triathlon Globalization Implant System for individual patients receiving primary total knee…
Category
Medical Device
Distribution
Distributed nationwide