Product Recalls in Oregon

Product recalls affecting Oregon — including food, drugs, consumer products, medical devices, and vehicles distributed to Oregon. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,681 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,681 in last 12 months

Showing 29813000 of 28,488 recalls

Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Stryker Corporation

Recalled Item: 1.2mm Cross Cut Fissure - Intended for use in the cutting Recalled by...

The Issue: May exhibit endotoxin levels greater than 2.15 EU/device, fever and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Luminex Molecular Diagnostics Inc

Recalled Item: NxTAG Respiratory Pathogen Panel +SARS-CoV-2 Recalled by Luminex Molecular...

The Issue: Respiratory pathogen panel may report an elevated rate (7.6% predicted...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Luminex Molecular Diagnostics Inc

Recalled Item: NxTAG Respiratory Pathogen Panel Recalled by Luminex Molecular Diagnostics...

The Issue: Respiratory pathogen panel may report an elevated rate (7.6% predicted...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· Bard Peripheral Vascular Inc

Recalled Item: The EVSRF catheter is a sterile Recalled by Bard Peripheral Vascular Inc Due...

The Issue: The Venclose" RF Ablation Catheters may have been manufactured with internal...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline CENTRAL CATHETER INSERTION TRA Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: It has been determined that certain Convenience kits that were packaged in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline TUBAL LIGATION PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: It has been determined that certain Convenience kits that were packaged in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing