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. 1,056 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
1,056 in last 12 months

Showing 16061–16080 of 28,744 recalls

Medical DeviceMay 25, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis with Laird Cooling Unit for SSFD: Material # Recalled by Siemens...

The Issue: Due to a defective sealing, coolant may inflow into the electrical parts of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee systems with Laird Cooling Unit for SSFD: Material Recalled by...

The Issue: Due to a defective sealing, coolant may inflow into the electrical parts of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Optima CT 540 Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Sorting-Drive Professional Part Recalled by Beckman Coulter Inc. Due to...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Revolution CT 160 1.5D STD WAUK Recalled by GE Healthcare, LLC Due to Some...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Intelligent Peri-Analytical Workstation (HW+SW) Recalled by Beckman Coulter...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery MI Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery RT labeled as: a. MID BJG Recalled by GE Healthcare, LLC Due to...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Sorting-Drive Product Part Recalled by Beckman Coulter Inc. Due to...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: CT Goldseal BrightSpeed 16 PWR TIO 2 YR Recalled by GE Healthcare, LLC Due...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery NM/CT 670 DR Recalled by GE Healthcare, LLC Due to When your...

The Issue: When your system was installed, the Main disconnect switch, EPO button on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery NM/CT 670 Pro Recalled by GE Healthcare, LLC Due to When your...

The Issue: When your system was installed, the Main disconnect switch, EPO button on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery NM/CT 670 ES Recalled by GE Healthcare, LLC Due to When your...

The Issue: When your system was installed, the Main disconnect switch, EPO button on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Draeger Medical, Inc.

Recalled Item: Fabius GS Tiro Anesthesia Machine Recalled by Draeger Medical, Inc. Due to...

The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Optima CT 520 Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery IQ 2.0 20cm Recalled by GE Healthcare, LLC Due to Some CT and...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery MI Digital Ready Recalled by GE Healthcare, LLC Due to DIGITAL...

The Issue: DIGITAL ReadyCT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Revolution EVO 3.6 Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing