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 2116121180 of 28,744 recalls

Medical DeviceJanuary 4, 2016· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue Measurement Module X1 Model: M3001A Recalled by Philips...

The Issue: The ST elevation alarm on the Patient Monitor or standalone X2 Measurement...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 31, 2015· Cordis Corporation

Recalled Item: CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes...

The Issue: Incorrect cannula of the sheath introducer (smaller than intended).

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 30, 2015· Leica Microsystems, Inc.

Recalled Item: This reagent is for in vitro diagnostic use. Pax-5 (1EW) Recalled by Leica...

The Issue: The Bond" Polymer Detection and Novolink" Polymer Detection System may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2015· Pharmacaribe llc

Recalled Item: PharmaCaribe PulmoSal 7% Sodium chloride Recalled by Pharmacaribe llc Due to...

The Issue: Vials were labeled as USP 7% Hypertonic saline instead of PulmoSal 7% (pH+)

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2015· Radiometer America Inc

Recalled Item: AQURE System Recalled by Radiometer America Inc Due to The AQURE System has...

The Issue: The AQURE System has a design error regarding sample type in which sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur PSA Assay Recalled by Siemens Healthcare Diagnostics, Inc Due...

The Issue: PSA assay is not meeting the High Dose Hook Effect expectation in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2015· Phadia Ab

Recalled Item: EliA SmDP Well Recalled by Phadia Ab Due to All equivocal and positive...

The Issue: All equivocal and positive results (greater or equal 7 EliA U/ml) on EliA...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2015· Viewray Incorporated

Recalled Item: MRIdian ViewRay Radiation Therapy System Recalled by Viewray Incorporated...

The Issue: The system loaded a completion fraction in the incorrect order after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M005489350 (XMD Recalled...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548880 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549550 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Endoscope ED-250XL5 Operations Manual: Cleaning Recalled by Fujifilm Medical...

The Issue: This correction is in response to publicized reports of multi-drug resistant...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Endoscope ED-450XL5 Operation Manual: Cleaning Recalled by Fujifilm Medical...

The Issue: This correction is in response to publicized reports of multi-drug resistant...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Endoscope ED-250XT5 Operations Manual: Cleaning Disinfection and Storage...

The Issue: This correction is in response to publicized reports of multi-drug resistant...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Endoscope Recalled by Fujifilm Medical Systems U.S.A., Inc. Due to This...

The Issue: This correction is in response to publicized reports of multi-drug resistant...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Endoscope ED-450XT5 Operation Manual: Cleaning Recalled by Fujifilm Medical...

The Issue: This correction is in response to publicized reports of multi-drug resistant...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· MOOG Medical Devices Group

Recalled Item: Moog Curlin Infusion Recalled by MOOG Medical Devices Group Due to Moog is...

The Issue: Moog is recalling Curlin 4000, 6000, and PainSmart Infusion Pumps...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548920 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548750 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548560 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing