Oregon recalls
4476 federal recalls on file affecting Oregon - 491 Oregon-specific plus 3985 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-08FDA-DeviceW L Gore & Associates, Inc.Class IINationwideGORE TAG thoracic endoprosthesis recalled for catheter separation
Due to catheter separation
- 2026-07-08FDA-DeviceMasimo CorporationClass IINationwideMasimo Radius VSM cuff recalled for false alarms and rough edges
Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal heart rate patients, which may distract clinicians away from management of true positive alarms, which could delay treatment; 2) Small and medium size blood pressure cuffs may contain rough edges, may result in skin irritation/redness.
- 2026-07-08FDA-DeviceMasimo CorporationClass IINationwideMasimo Radius VSM ECG set recalled for false alarms and cuff irritation
Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal heart rate patients, which may distract clinicians away from management of true positive alarms, which could delay treatment; 2) Small and medium size blood pressure cuffs may contain rough edges, may result in skin irritation/redness.
- 2026-07-08FDA-DeviceLaborie Medical Technologies CorpClass IINationwideLaborie Solar GI System recalled for moisture accumulation risk
Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing or at the hydrophobic filter and waterproof pressure sensors. Accumulated moisture may affect airflow or pressure measurement performance if not properly removed.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Access Systems biopsy trays recalled for defective lidocaine
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Provena Midline Catheters recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerPICC catheters recalled for lidocaine quality issue
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Groshong NXT catheter recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerPICC Provena catheters recalled for defective lidocaine
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerMidline Catheter recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerMidline Catheter recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Power-Trialysis dialysis catheters recalled for lidocaine defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Power-Trialysis dialysis catheters recalled for lidocaine defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerPICC SV catheters recalled for lidocaine defects
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard PowerPICC SOLO HF Catheter recalled for defective lidocaine
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard DuoGlide dialysis catheter recalled for defective lidocaine
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Poly Midline Catheter recalled for lidocaine manufacturing defects
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IINationwideBard Access Systems drainage trays recalled for lidocaine manufacturing defect
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
- 2026-07-08FDA-DeviceCovidien LLCClass IINationwideCovidien Shiley decannulation plug recalled for mislabeled DEHP
Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP.
- 2026-07-08FDA-DeviceCarl Zeiss MeditecClass IINationwideZeiss Intrabeam radiation applicator recalled for manufacturing defect
Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications.
- 2026-07-08FDA-DeviceSiemensClass IINationwideSiemens ARTIS icono ceiling monitor recalled for loose screws
Potential issue with the Display ceiling suspension (DCS Fix XL) that holds the monitor in place. Over time some screws that keep the monitor attached to the suspension may gradually loosen.
- 2026-07-08FDA-DeviceRaysearch LaboratoriesClass IINationwideRayCare 2024A SP4 recalled for beam delivery note data loss
Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the user is not notified of the change.
- 2026-07-08FDA-DeviceRaysearch LaboratoriesClass IINationwideRayCare 2024A SP1 recalled for beam note data loss risk
Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the user is not notified of the change.
- 2026-07-08FDA-DeviceMedela IncClass IIMedela ENFit ExSet extension set recalled for connector incompatibility
May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue could lead to slight delay in delivery of enteral nutritional fluids or oral medication.
- 2026-07-08FDA-DeviceAccuray IncorporatedClass IINationwideAccuray Cyberknife recalled for collimator fall risk
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room control pendant, the collimator may release and fall from the housing.
- 2026-07-08FDA-DeviceSiemensClass IINationwideSiemens ARTIS icono floor recalled for movement capability loss
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
- 2026-07-08FDA-DeviceSiemensClass IINationwideSiemens ARTIS icono ceiling recalled for movement loss risk
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
- 2026-07-08FDA-DeviceSiemensClass IINationwideSiemens ARTIS icono biplane recalled for movement loss risk
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
- 2026-07-08FDA-DeviceAccuray IncorporatedClass IINationwideAccuray Cyberknife recalled for collimator drop risk
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room control pendant, the collimator may release and fall from the housing.
- 2026-07-08FDA-DeviceTELEFLEX LLCClass IINationwidePilling Wecksorb Neurosponges recalled for endotoxin contamination
Due to out-of-specification, or potential out-of-specification, levels of endotoxins
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