Product Recalls in Wisconsin

Product recalls affecting Wisconsin — including food, drugs, consumer products, medical devices, and vehicles distributed to Wisconsin. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,736 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,736 in last 12 months

Showing 30013020 of 28,744 recalls

Medical DeviceSeptember 9, 2024· Atrium Medical Corporation

Recalled Item: iCast Covered Stent Recalled by Atrium Medical Corporation Due to There is...

The Issue: There is an error in the Unique Device Identifier (UDI) printed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2024· Enchroma Inc

Recalled Item: EnChroma Safety Glasses with Rx Indoor Universal Lenses: Martinez Cx1 Indoor...

The Issue: Safety glasses with Rx indoor universal lenses fail to meet high impact...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2024· SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION

Recalled Item: SONIALVISION G4 is a multi-purpose X-ray R/F system. The equipment Recalled...

The Issue: X-ray R/F system software with certain versions of the control board may...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2024· SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION

Recalled Item: The FLUOROspeed is intended to be used as a universal Recalled by SHIMADZU...

The Issue: X-ray R/F system software with certain versions of the control board may...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2024· SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION

Recalled Item: Trinias unity Recalled by SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Due...

The Issue: If digital angiography system is used with a specific catheterization table...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific myLUX Patient Application for an Apple Mobile device...

The Issue: Patients using the Model 2939 myLUX Patient Application on their Apple...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2024· Agfa Healthcare NV

Recalled Item: Enterprise Imaging XERO Viewer- software application used for and Recalled...

The Issue: Software defect, when an image has non-square pixel spacing, the /localizer...

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 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