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. 1,917 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls

1,917 in last 12 months

All Food Drug Medical Device Consumer Product Vehicle

Showing 26741–26760 of 52,482 recalls

Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Percepta Quad CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm...

The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...

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

Class II — Potential Health HazardOngoing

Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Percepta Quad CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm...

The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...

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

Class II — Potential Health HazardOngoing

Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...

The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...

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

Class II — Potential Health HazardOngoing

Medical DeviceJune 21, 2018· Becton Dickinson & Co.

Recalled Item: BD BBL GC-Lect Agar Recalled by Becton Dickinson & Co. Due to A portion of...

The Issue: A portion of this lot was manufactured using Gentamicin instead of...

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

Class II — Potential Health HazardOngoing

Medical DeviceJune 21, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...

The Issue: The flow rate test verification was not properly executed for certain Sigma...

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

Class II — Potential Health HazardOngoing

Medical DeviceJune 20, 2018· Vyaire Medical

Recalled Item: The Tri-Flo Subglottic Suction System Recalled by Vyaire Medical Due to...

The Issue: Vyaire Medical has discovered potential patient safety risk with associated...

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

Class I — Serious Health HazardOngoing

Medical DeviceJune 20, 2018· Boston Scientific Corporation

Recalled Item: Boston Scientific Maestro 4000 Cardiac Ablation System Recalled by Boston...

The Issue: Reports of unintended continuation of radiofrequency (RF) energy delivery...

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

Class II — Potential Health HazardOngoing

Medical DeviceJune 20, 2018· Espiner Medical Ltd

Recalled Item: Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml...

The Issue: Label was incorrect. The label states that the volume of the retrieval bag...

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

Class II — Potential Health HazardOngoing

DrugJune 20, 2018· Gaia Ethnobotanical LLC

Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...

The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...