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. 2,570 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,570 in last 12 months

Showing 1888118900 of 28,744 recalls

Medical DeviceFebruary 27, 2017· LIEBEL-FLARSHEIM COMPANY LLC

Recalled Item: Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim...

The Issue: Software issue. The difference between the display and dosimeter readings In...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT model number 882482 BrightView and BrightView X are Recalled...

The Issue: The brake hub was not engaging with the gear box shaft due to an error in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X 3/8 model number 882478 BrightView and BrightView X Recalled by...

The Issue: The brake hub was not engaging with the gear box shaft due to an error in...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 24, 2017· Philips North America, LLC

Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips North America, LLC...

The Issue: HeartStart MRx Monitor/Defibrillator may may exhibit abnormal behavior when...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 24, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView SPECT model number 882480 BrightView and BrightView X are...

The Issue: The brake hub was not engaging with the gear box shaft due to an error in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X 3/4 model number 882479 BrightView and BrightView X Recalled by...

The Issue: The brake hub was not engaging with the gear box shaft due to an error in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Radiology CT - 728244 Computed Tomography X-ray systems...

The Issue: Philips identified a 4D CT pulmonary phase issue on Brilliance BigBore...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Streck

Recalled Item: Cyto-Chex BCT - blood specimen collection device - Immunophenotyping...

The Issue: Complaints of the 2.0ml tube stopper coming loose during phlebotomy when...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Enzyme 2 Calibrator Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has confirmed a positive bias of up to 41% in...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 23, 2017· Hill-Rom, Inc.

Recalled Item: TotalCare Bed Systems Recalled by Hill-Rom, Inc. Due to The bed exit alarm...

The Issue: The bed exit alarm may not function properly if the alarm has been armed for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Oncology CT - 728243 Computed Tomography X-ray systems...

The Issue: When the user performs a retrospective respiratory gated 4D CT scan with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: JAMSHIDI (TJ) NEEDLE BONE MARROW [a.) 13G x 3.5 Recalled by Carefusion 2200...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: JAMSHIDI (TJ) NEEDLE BM ASP MAC [a.) 13G x 3.5 Recalled by Carefusion 2200...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: JAMSHIDI NEEDLE BIOPSY [15G X 100MM DISP Recalled by Carefusion 2200 Inc Due...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: Thoracentesis/ Paracentesis Kit 10/CS Recalled by Carefusion 2200 Inc Due to...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: Manometer Recalled by Carefusion 2200 Inc Due to The integrity of the...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: ILLINOIS (TJ) NEEDLE ASPIRATION [15GA Recalled by Carefusion 2200 Inc Due to...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2017· Ace Surgical Supply Co., Inc.

Recalled Item: INFINITY Internal Hex Healing Abutment Recalled by Ace Surgical Supply Co.,...

The Issue: Incorrect device was packaged.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA, Inc

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

The Issue: Software updates

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 16 TruePoint TrueV - 4R Recalled by Siemens Medical Solutions USA...

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing