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.

24176–24200 of 81019

SevereFDA (Drugs)·D-0318-2022·2022-01-05
SterRx Morphine Sulfate Injection Recalled for Sterility Assurance
SterRx is recalling 880 bags of Morphine Sulfate in 0.9% Sodium Chloride Injection nationwide due to lack of assurance of sterility. Patients and healthcare providers should stop using affected units immediately.
Product
MORPHINE SULFATE, in 0.9% Sodium Chloride Injection, 50 mg per 50 mL, (1 mg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-427-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0301-2022·2022-01-05
SterRx Morphine Sulfate Injection Recalled for Sterility Assurance
SterRx is recalling Morphine Sulfate in 0.9% Sodium Chloride Injection (1 mg per mL) nationwide due to lack of assurance of sterility. The recall affects 880 units distributed across the United States.
Product
Morphine Sulfate in 0.9% Sodium Chloride Injection, 100 mg per 100 mL (1 mg per mL), Rx only, SterRx, 141 Idaho Avenue, Plattsburgh, NY, 12903, NDC 70324-427-02.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0312-2022·2022-01-05
Midazolam Injection Recalled Due to Lack of Sterility Assurance
SterRx is recalling Midazolam in 0.9% Sodium Chloride Injection nationwide due to lack of assurance of sterility. The recall affects approximately 36,360 bags distributed across the United States.
Product
Midazolam in 0.9% Sodium Chloride Injection, 100 mg per 100 mL (1 mg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-102-02.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0303-2022·2022-01-05
SterRx Norepinephrine Injection Recalled Due to Sterility Assurance Concerns
SterRx is recalling 9,360 bags of Norepinephrine 4 mg per 250 mL injection nationwide due to lack of assurance of sterility. The product is used in hospital and clinical settings to treat low blood pressure.
Product
NOREPINEPHRINE 4 mg per 250 mL (16 mcg per mL) in 5% Dextrose Injection, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-451-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0320-2022·2022-01-05
SterRx Norepinephrine Injection Recalled Due to Lack of Sterility Assurance
SterRx is recalling 121,584 bags of Norepinephrine 4 mg per 250 mL injection nationwide due to lack of assurance of sterility. The drug is used to treat low blood pressure in critical care settings.
Product
NOREPINEPHRINE, 4 mg per 250 mL, (18 mcg per mL) in 0.9% Sodium Chloride Injection, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-651-01.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0418-2022·2022-01-05
Percept PC Implantable Neurostimulator May Become Unresponsive During Cardioversion
The Model B35200 Percept PC Neurostimulator may become unresponsive during cardioversion procedures when circuit electronics are damaged. Affected patients should contact their healthcare provider.
Product
Model B35200 - Percept PC BrainSense Implantable Neurostimulator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0441-2022·2022-01-05
Cancer treatment linear accelerator systems recalled for wrong-site dosing risk
Siemens recalled 13 ARTISTE linear accelerator systems for cancer treatment due to a potential safety issue that could cause radiation to be delivered to the wrong treatment site.
Product
ARTISTE with syngo RT Therapist-linear accelerator systems to deliver X-Ray photon and electron radiation for the therapeutic treatment of cancer. Model Number: 8162815
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0440-2022·2022-01-05
Siemens Atellica CH β2-Microglobulin Assay Lot 211446 Recalled for Measurement Bias
Siemens Healthcare Diagnostics recalled lot 211446 of the Atellica CH β2-Microglobulin assay due to analytical bias in test results. The assay showed positive bias up to 20.9% at some concentrations and negative bias up to 10.5% at others.
Product
Atellica CH ¿2-Microglobulin (B2M) -M) Assay for in vitro diagnostic use in the quantitative determination of ¿2-microglobulin in human serum and plasma Siemens Material Number (SMN): 11097635
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0426-2022·2022-01-05
VIDAS Clostridium Difficile GDH test substrate error causes test failure
bioMerieux recalls VIDAS Clostridium Difficile GDH diagnostic test kits due to a substrate error that prevents test execution. Affected users must retest samples, potentially delaying results.
Product
VIDAS Clostridium Difficile GDH, REF 30125-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0443-2022·2022-01-05
Medical Device Aberrometer Systems Affected by Remote Code Execution Vulnerability
AMO Manufacturing's iDesign aberrometer systems (711 units, Models G300 and G301) are vulnerable to remote code execution through the Windows Print Spooler service. An attacker could run arbitrary code with SYSTEM privileges to install programs, access or delete data, or create accounts.
Product
iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan Studio (United States); iDesign Refractive Studio Aberrometer (International) and (United States), Model: G301
Category
Medical Device
Distribution
47 states
HighCPSC·22043·2022-01-05
CRT Motor Youth All-Terrain Vehicles Recalled for Crash Hazard
CRT Motor is recalling about 100 youth ATVs sold at Motorsports Planet because they do not meet mandatory safety requirements and can exceed maximum speed, increasing crash risk.
Product
CRT Motor Youth All-Terrain Vehicles (ATVs)
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0419-2022·2022-01-05
da Vinci SP Surgical System Software Energy Delivery Defect
Intuitive Surgical recalls 46 da Vinci SP Surgical systems due to software defect causing potential failure or inadvertent delivery of surgical energy. Issue may require surgeon intervention during procedures.
Product
da Vinci SP Surgical systems with the following Model Name/ Model Number / UDI: ASSY,PSS,SP1098,P4/ 380601-44/ 00886874114605 ASSY,SSC,SP1098,P4/ 380940-44 / 00886874114735 ASSY,VSS,SP1098,P4/ 380941-44 / 00886874114742 SOFTWARE, SYSTEM EMBEDDED RLS, SP1098, B70_P4_B327 (OS4…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0322-2022·2022-01-05
Norepinephrine Injection Recalled Due to Lack of Sterility Assurance
SterRx is recalling 36,576 bags of Norepinephrine 16 mg per 250 mL injection (0.9% Sodium Chloride) distributed nationwide because the manufacturer cannot assure the product meets sterility requirements.
Product
NOREPINEPHRINE, 16 mg per 250 mL, (64 mcg per mL) in 0.9% Sodium Chloride Injection, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-926-01.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0307-2022·2022-01-05
SterRx Succinylcholine Chloride Injection Recalled for Sterility Assurance
SterRx is recalling Succinylcholine Chloride Injection 20 mg/mL vials (1,000 mL) distributed nationwide due to lack of assurance of sterility. The 3,540 affected bags may pose a risk to patients receiving this injectable drug.
Product
Succinylcholine Chloride Injection, 200 mg per 10 mL (20 mg per mL), 1,000 mL, Rx only, SterRx, 141 Idaho Avenue, Plattsburgh, NY 12903, NDC 70324-826-01.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0425-2022·2022-01-05
VIDAS diagnostic test for C. difficile recalled due to substrate defect
bioMerieux's VIDAS Clostridium difficile diagnostic test is being recalled due to a substrate error that prevents the test from running. Users must re-test samples, potentially delaying diagnosis.
Product
VIDAS Clostridium Difficile Toxin A&B, CDAB,REF 30118-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0442-2022·2022-01-05
Karl Storz Endoscope Sterilization Trays Instructions for Use Updated
Karl Storz Udel Sterilization Tray instructions for use have been updated to correct sterilization methods and clarify endoscope compatibility. Ethylene oxide is now excluded as a sterilization modality.
Product
Karl Storz Udel Sterilization Tray Instructions for Use, Tray Part Number/Description: 39301ACTS/CAMERA TRAY (STERRAD, INLINE CAMERA HEADS); 39301AS/RIGID TELESCOPE TRAY (STERRAD, 2 RIGID SCOPES 4MM X 18CM); 39301BCTS/CAMERA TRAY (INLINE/C-MOUNT CAMERA HEADS); 39301BS/RIGID…
Category
Medical Device
Distribution
51 states
HighFDA (Devices)·Z-0444-2022·2022-01-05
Catalys Precision Laser System recalled for remote code execution vulnerability
AMO Manufacturing is recalling Catalys Precision Laser Systems due to a Windows Print Spooler vulnerability that could allow unauthorized remote code execution with system privileges.
Product
Catalys Precision Laser System, Models: Catalys-U (United States), Catalys-I (International), Catalys-C (China); and Catalys Precision Laser System No Bed, Models: 0160-6020 (United States), 0160-6010 (International)
Category
Medical Device
Distribution
47 states
HighFDA (Devices)·Z-0420-2022·2022-01-05
Ultimum Hemostasis Introducer devices recalled due to manufacturing error
Abbott is recalling one lot of Ultimum Hemostasis Introducer devices due to a manufacturing error that resulted in incorrect hub and length. Affected devices are 12 cm long instead of the intended 5 cm.
Product
Ultimum HEMOSTASIS INTRODUCER 5f 1.67 MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0324-2022·2022-01-05
SterRx Phenylephrine HCl Injection Recalled for Sterility Assurance Failure
SterRx is recalling phenylephrine HCl injectable solution nationwide due to lack of assurance of sterility. The affected product is a 50 mg per 250 mL injection in 0.9% sodium chloride.
Product
PHENYLephrine HCl, 50 mg per 250 mL, (200 mg per mL) in 0.9% Sodium Chloride Injection, Rx Only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-901-01.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0437-2022·2022-01-05
VIDAS Lyme diagnostic test device recalled due to substrate error
bioMerieux recalled VIDAS Lyme IgG II test devices (two lots) due to a substrate error that prevents tests from running. Users must retest patients, potentially delaying Lyme disease diagnosis.
Product
VIDAS Lyme IgG II (LYM), REF 417401
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0423-2022·2022-01-05
Speech Generation Device Charging Components Recalled for Fire and Electric Shock Hazard
Forbes Rehab Services is recalling Monoprice charging cables and iClever charging bricks for ProSlate Speech Generation Devices due to fire and electric shock risks if cables are damaged or charging occurs near moisture.
Product
Affected components are limited to the Monoprice charging cable (Product # 4867) and 24W iClever Boost Cube charging brick components for the SoundPOD Bluetooth Speaker accessory to the ProSlate Speech Generation Devices (including Proslate 13: B398PS130; Proslate 10: B398PS100…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0429-2022·2022-01-05
VIDAS Mumps IgG diagnostic test kit recalled due to substrate error
bioMerieux is recalling one lot of VIDAS Mumps IgG diagnostic tests because a substrate error prevents the tests from running, causing delays.
Product
VIDAS Mumps IgG (MPG), REF 30218
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0428-2022·2022-01-05
VIDAS procalcitonin diagnostic test substrate error causes testing delays
Nationwide recall of VIDAS procalcitonin test kits for substrate defects that prevent testing and require retesting, potentially delaying diagnostic results.
Product
VIDAS B.R.A.H.M.S. PROCALCITONIN PCT, REF 30450-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0435-2022·2022-01-05
VIDAS Estradiol II Test Device Recalled Due to Substrate Error
bioMerieux is recalling one lot of VIDAS Estradiol II diagnostic test devices due to a substrate error that prevents tests from running, causing delayed results and requiring repeat testing.
Product
VIDAS Estradiol II, REF 30431-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0439-2022·2022-01-05
VIDAS SARS-COV-2 Diagnostic Test Recalled for Substrate Error
bioMerieux is recalling two lots of VIDAS SARS-COV-2 IgG diagnostic tests due to substrate errors that prevent test execution, requiring users to repeat testing and potentially delaying results.
Product
VIDAS SARS-COV-2 IgG, Ref 423834-01
Category
Medical Device
Distribution
Distributed nationwide