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. 2,557 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,557 in last 12 months

Showing 2028120300 of 28,744 recalls

Medical DeviceMay 16, 2016· Lifeline First Aid LLC

Recalled Item: 5195GM Recalled by Lifeline First Aid LLC Due to Cadillac First Aid Kit is...

The Issue: Cadillac First Aid Kit is recalled because it contains the CPR Shield with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2016· Ortho-Clinical Diagnostics

Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics...

The Issue: If the user selects the Comment or Interpretation option (in the enGEN .gsb...

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

Class III — Low RiskOngoing
Medical DeviceMay 12, 2016· Baxter Healthcare Corp

Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...

The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2016· CareFusion 303, Inc.

Recalled Item: Alaris System PC Unit Model 8015 with software versions 9.17 and 9.19...

The Issue: A patient weight can be populated incorrectly under certain conditions when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2016· Baxter Healthcare Corp

Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...

The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2016· Baxter Healthcare Corp

Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...

The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2016· Zimmer Biomet, Inc.

Recalled Item: Persona Trabecular Metal Tibia Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Zimmer Inc. is initiating a recall of specific Persona" Trabecular Metal"...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2016· Synthes (USA) Products LLC

Recalled Item: Norian Drillable Inject 3 CC-Sterile Recalled by Synthes (USA) Products LLC...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2016· Siemens Healthcare Diagnostics Inc.

Recalled Item: Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or...

The Issue: Premature bucket failures

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2016· Synthes (USA) Products LLC

Recalled Item: Norian Drillable Inject 5 CC-Sterile Recalled by Synthes (USA) Products LLC...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2016· Synthes (USA) Products LLC

Recalled Item: Norian Drillable Inject 10 CC-Sterile Recalled by Synthes (USA) Products LLC...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2016· Medical Vision Ab

Recalled Item: Double Pump RF Patient Cassette Recalled by Medical Vision Ab Due to...

The Issue: Sterility of device may be compromised due to sterile package breakage.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· GE Healthcare, LLC

Recalled Item: Optima 1.5T MR430s MR Scanner Recalled by GE Healthcare, LLC Due to The gas...

The Issue: The gas venting may not occur properly. A site reported a magnet quenching...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software error in previous software versions in which two for the same image...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· GE Healthcare, LLC

Recalled Item: GE Revolution CT The system is intended for head Recalled by GE Healthcare,...

The Issue: GEHC has become aware of a potential safety issue in the Revolution CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· Immuno-Mycologics, Inc

Recalled Item: Histoplasma Yeast Complement Fixation Antigen Dilute Ref# H30150 The fungal...

The Issue: The device was found to have bacterial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· GE Healthcare, LLC

Recalled Item: MSK 1.5T Extreme MR Scanner Recalled by GE Healthcare, LLC Due to The gas...

The Issue: The gas venting may not occur properly. A site reported a magnet quenching...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products AFP Reagent Pack Recalled by ORTHO-CLINICAL...

The Issue: Ortho Clinical Diagnostics (OCD) confirmed that specific lots of VITROS...

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

Class III — Low RiskOngoing
Medical DeviceMay 6, 2016· Invivo Corporation

Recalled Item: Invivo Sentinelle Venguard Breast MRI Auxiliary Table/Tabletop with 8/16...

The Issue: A diode was inadvertently not assembled into the system, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2016· BEST THERATRONICS LTD.

Recalled Item: Best Theratronics cabinet x-ray systems intended for use in the Recalled by...

The Issue: It was discovered that both the new device and the predicate device failed...

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

Class II — Potential Health HazardOngoing