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. 2,109 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,109 in last 12 months

Showing 44614480 of 50,914 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· 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 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 4, 2024· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica Biosystems Cryostat Model Number CM1100 Recalled by LEICA BIOSYSTEMS...

The Issue: As part of our post market surveillance, we recognized that some customers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica Biosystems Cryostat Model Number CM1850 Recalled by LEICA BIOSYSTEMS...

The Issue: As part of our post market surveillance, we recognized that some customers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· Howmedica Osteonics Corp.

Recalled Item: Triathlon Universal TS Baseplate Size 2 - A single use Recalled by Howmedica...

The Issue: Anterior locking tabs on the Triathlon Universal Baseplate are out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica Biosystems Cryostat Model Number CM1950 Recalled by LEICA BIOSYSTEMS...

The Issue: As part of our post market surveillance, we recognized that some customers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica Biosystems Cryostat Model Number CM3050 S Recalled by LEICA BIOSYSTEMS...

The Issue: As part of our post market surveillance, we recognized that some customers...

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

Class II — Potential Health HazardOngoing