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. 2,736 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,736 in last 12 months

Showing 21012120 of 28,744 recalls

Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as UNIVERSAL DAVINCI ROBOTIC P. Sterile surgical...

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as HEAD AND NECK OSIS Recalled by MEDLINE INDUSTRIES,...

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as MINOR PACK and LAPAROSCOPY. Sterile surgical drape....

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as ENT-PLASTICS PACK. Sterile surgical drape. Recalled...

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as DRAPE C-SECTION W/ WINDOW Recalled by MEDLINE...

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as FACE LIFT. Sterile surgical drape. Recalled by...

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· ZOLL Medical Corporation

Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...

The Issue: The potential for devices to fail their self-test as a result of prolonged...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· ZOLL Medical Corporation

Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...

The Issue: The potential for devices to fail their self-test as a result of prolonged...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· ZOLL Medical Corporation

Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...

The Issue: The potential for devices to fail their self-test as a result of prolonged...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· ZOLL Medical Corporation

Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...

The Issue: The potential for devices to fail their self-test as a result of prolonged...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· ZOLL Medical Corporation

Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...

The Issue: The potential for devices to fail their self-test as a result of prolonged...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· ZOLL Medical Corporation

Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...

The Issue: The potential for devices to fail their self-test as a result of prolonged...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· Smiths Medical ASD, Inc.

Recalled Item: Portex Endotracheal Tube Recalled by Smiths Medical ASD, Inc. Due to...

The Issue: Affected devices have a smaller diameter than expected and may potentially...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 13, 2025· ZOLL Medical Corporation

Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...

The Issue: The potential for devices to fail their self-test as a result of prolonged...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· ZOLL Medical Corporation

Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...

The Issue: The potential for devices to fail their self-test as a result of prolonged...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· Remel, Inc

Recalled Item: remel BLOOD AGAR EMB AGAR BIPLATE Recalled by Remel, Inc Due to Potential...

The Issue: Product may contain surface and subsurface contamination of Listeria...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· Remel, Inc

Recalled Item: remel BLOOD AGAR MacCONKEY AGAR BIPLATE Recalled by Remel, Inc Due to...

The Issue: Product may contain surface and subsurface contamination of Listeria...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: namic convenience kits labeled as: 1) MTS Recalled by MEDLINE INDUSTRIES, LP...

The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: namic convenience kits labeled as: PML Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: namic convenience kits labeled as: MTS Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...

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

Class II — Potential Health HazardOngoing