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 2046120480 of 28,744 recalls

Medical DeviceApril 8, 2016· Merge Healthcare, Inc.

Recalled Item: DR Systems Unity PACS software Recalled by Merge Healthcare, Inc. Due to The...

The Issue: The software is not adding the correct tomo image.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics confirmed a software timing anomaly in which the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Skytron, Div. The KMW Group, Inc

Recalled Item: EZ Slide Battery/line powered hydraulic table with removable leg section...

The Issue: The potential exists within the identified tables that incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Ortho Clinical Diagnostics confirmed a software timing anomaly in which the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Signmoidoscope Product Usage: Intended to provide optical visualization of...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Colonoscope Product Usage: Intended to provide optical visualization of and...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Ultrasound Gastroscope Product Usage: Intended to provide optical...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Gastroscope Product Usage: Intended to provide optical visualization of and...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Duodenoscope Product Usage: Intended to provide optical visualization of and...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Confocal GI Scope Product Usage: Intended to provide optical visualization...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2016· Ceg Enterprises Llc

Recalled Item: Germ Terminator Recalled by Ceg Enterprises Llc Due to CEG Enterprises, LLC...

The Issue: CEG Enterprises, LLC is recalling Germ Terminator Toothbrush Sanitizer GT100...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: MasimoSET LNOP DCI adult SpO2 reusable sensor Recalled by Merge Healthcare,...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare....

The Issue: Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. The firm name on the label is Merge Healthcare...

The Issue: When taking measurements from images on the Cardio workstation or from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare Recalled...

The Issue: Potential exists for an incorrect patient image being displayed which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Station and Merge Eye Care PACS. Recalled by Merge Healthcare,...

The Issue: During an antivirus program scan of the Eye Station or Eye Care PACS, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Hemo software. The firm name on the labeling is Merge Healthcare...

The Issue: Use of the software may show an incorrect value to the user when viewing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Masimo SPO2 Sensor Recalled by Merge Healthcare, Inc. Due to Under certain...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive (ICEA) software. The firm name on the Recalled...

The Issue: An error message can occur resulting in the prior studies being unavailable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: SpO2 connecting cable for Masimo LNCS sensor (Merge Part Number:...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing