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. 2,662 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,662 in last 12 months

Showing 1250112520 of 28,744 recalls

Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Healthineers Ysio Max - Interventional Fluoroscopic X-Ray System...

The Issue: Two software issues (1) Using the override function in case of blocked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Healthineers Luminos Agile Max Model: 10762472 - Product Usage:...

The Issue: Two software issues (1) Using the override function in case of blocked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Healthineers Luminos dRF Max Model: 10762471- Product Usage: is...

The Issue: Two software issues (1) Using the override function in case of blocked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Ysio Max Recalled by Siemens Medical Solutions USA, Inc Due to A software...

The Issue: A software bug may lead to one image to be assigned to two different...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens became aware of an issue of incorrect use of the bypass key...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A software bug may lead to one image to be assigned to two different...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens became aware of an issue of incorrect use of the bypass key...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A software bug may lead to one image to be assigned to two different...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Uroskop Omnia max Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens became aware of an issue of incorrect use of the bypass key...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Stryker Corporation

Recalled Item: Spy-Phi Drape (HH2000) sold as a Spy-Phi Pack (HH9006). Only Recalled by...

The Issue: Sterile drapes packaged in an unsealed pouch.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Stryker Corporation

Recalled Item: Spy-Phi Drape only (HH2020) Pack of 20 HH2000 (Sold internationally Recalled...

The Issue: Sterile drapes packaged in an unsealed pouch.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· CME America, LLC

Recalled Item: CME America BodyGuard Infusion Pump System Recalled by CME America, LLC Due...

The Issue: Infusion Pump Systems may have a delivery inaccuracy of up to 13%, which may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 7, 2020· Zimmer Biomet, Inc.

Recalled Item: THP Hip Plating System Recalled by Zimmer Biomet, Inc. Due to Potential...

The Issue: Potential increase in fracture rate was detected during internal testing, in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Care Essentials Pty., Ltd.

Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...

The Issue: Potential for thermal damage near the power cord connector and Power Entry...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Care Essentials Pty., Ltd.

Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...

The Issue: Potential for thermal damage near the power cord connector and Power Entry...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Palodex Group Oy

Recalled Item: Instrumentarium Dental Express SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL...

The Issue: Slow degradation of plastic insulation used in the PSU DC plug of the DIGORA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Palodex Group Oy

Recalled Item: Gendex GXPS-500 SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER)...

The Issue: Slow degradation of plastic insulation used in the PSU DC plug of the DIGORA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Palodex Group Oy

Recalled Item: Soredex DIGORA Optime SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER)...

The Issue: Slow degradation of plastic insulation used in the PSU DC plug of the DIGORA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Palodex Group Oy

Recalled Item: KaVo Scan eXam SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER) Recalled...

The Issue: Slow degradation of plastic insulation used in the PSU DC plug of the DIGORA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Humidity Pack (Qty 5) Recalled by Siemens Healthcare...

The Issue: A software error is causing the analyzer to incorrectly eject affected...

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

Class II — Potential Health HazardOngoing