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. 1,078 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
1,078 in last 12 months

Showing 14041–14060 of 28,744 recalls

Medical DeviceApril 22, 2019· Cook Inc.

Recalled Item: Cook Kwart Retro-Inject Ureteral Stent Set: PRODUCT/CATALOG NUMBER/GPN: 4.7...

The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Temp Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS4 Government Bundle Recalled by Philips North America, LLC Due...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS4 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Ethicon, Inc.

Recalled Item: ETHIBOND EXCEL ETHIBOND Polvester Suture-Green 75cm USP1 Single Armed CTX...

The Issue: Possibility that a suture raw material containing high endotoxin levels was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Ethicon, Inc.

Recalled Item: ETHIBOND EXCEL¿ Polyester Suture-ETHIBOND Green 75cm USP1 Single Armed CT-1...

The Issue: Possibility that a suture raw material containing high endotoxin levels was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips Healthcare Informatics, Inc.

Recalled Item: IntelliSpace PACS 4.4 Recalled by Philips Healthcare Informatics, Inc. Due...

The Issue: Images may potentially become corrupt while using the system.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· AURIS HEALTH INC

Recalled Item: Monarch Recalled by AURIS HEALTH INC Due to Reports of aspirating biopsy...

The Issue: Reports of aspirating biopsy needle breakage

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-TOP 24202 ADULT ECC Material: 701054295R01 Recalled by...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-T 52301 ¿ Sash & Accessory Pack Material: 709000266...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-T 4903 Mercy Med w/o Oxy Material:701066664 Recalled by...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-T 8805 ECC PACK Material: 701053361 Recalled by Maquet...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-TOP 33704 ECC 1/4" PACK Material: 701054150 Recalled by...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-T 8030 4 in High Flow Pigtail Material: 709000366 Recalled by...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-TOP 27901 SMALL PATIENT CI Material:701052287 Recalled by...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing