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 25212540 of 28,744 recalls

Medical DeviceNovember 25, 2024· Angiodynamics, Inc.

Recalled Item: AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number:...

The Issue: Potential for procedural delays or interruptions during use of the Auryon...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Spacelabs Healthcare, Inc.

Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...

The Issue: Telemetry receiver systems may experience a Windows proxy Issue causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Spacelabs Healthcare, Inc.

Recalled Item: Xhibit Telemetry Receiver with Software Recalled by Spacelabs Healthcare,...

The Issue: Telemetry receivers with affected software versions may experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Spacelabs Healthcare, Ltd.

Recalled Item: Eclipse PRO The Spacelabs model 98700 is a Recalled by Spacelabs Healthcare,...

The Issue: Due to a manufacturing error the incorrect device serial number was...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Spacelabs Healthcare, Ltd.

Recalled Item: Eclipse Mini The Eclipse MINI Model 98900 is Recalled by Spacelabs...

The Issue: Due to a manufacturing error the incorrect device serial number was...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Spectranetics Corporation

Recalled Item: Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code Recalled...

The Issue: Due to complaints received for the marker band detaching from the distal tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 9mm - Silicone Recalled by Adept...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 6mm - Double - Silicone Recalled by...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - Donaldson - Blue Silicone Recalled by Adept...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 9mm - Double - Silicone Recalled by...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 12mm - Silicone Recalled by Adept...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 6mm - Silicone Recalled by Adept...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 12mm - Double - Silicone Recalled by...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - Donaldson - Double - Blue Silicone Recalled by...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· 3M Company - Health Care Business

Recalled Item: Clarity Precision Grip Attachments Recalled by 3M Company - Health Care...

The Issue: Attachments may not mate with the tooth as intended in the digital treatment...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing