Product Recalls in Kansas

Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,085 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,085 in last 12 months

Showing 44014420 of 50,117 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· 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 5, 2024· Beckman Coulter, Inc.

Recalled Item: Access Thyroglobulin Antibody II Recalled by Beckman Coulter, Inc. Due to...

The Issue: IFUs for the device incorrectly states the biotin interference was...

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 brand medical procedure convenience kits Recalled by MEDLINE...

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: Centurion PEDIATRIC/ADULT TRACHEOSTOMY T 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· B-K Medical A/S

Recalled Item: bk3000 Recalled by B-K Medical A/S Due to The internal power connections at...

The Issue: The internal power connections at the power inlet of the ultrasound devices...

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 CM1510 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