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. 2,715 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,715 in last 12 months

Showing 44214440 of 28,744 recalls

Medical DeviceMarch 14, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Sterile convenience kit: Medline Birthing Room Pack Recalled by MEDLINE...

The Issue: Surgical convenience kits containing Pure Pouch component that has weak...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Sterile surgical convenience kit: Medline Retrograde PK-22025203-LF Recalled...

The Issue: Surgical convenience kits containing Pure Pouch component that has weak...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2024· Merit Medical Systems, Inc.

Recalled Item: Prelude Guide Sheath Roadster Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Their is a potential that sheaths labeled with .018 dilators may contain a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2024· Merit Medical Systems, Inc.

Recalled Item: Prelude Guide Sheath Roadster Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Their is a potential that sheaths labeled with .018 dilators may contain a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2024· Johnson & Johnson Surgical Vision, Inc.

Recalled Item: Johnson & Johnson VISION Reusable LAMINAR High Flow Irrigation Sleeve...

The Issue: Due to a manufacturing variation of the irrigation sleeves which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2024· Allergan Sales, LLC

Recalled Item: Keller Funnel 2 Recalled by Allergan Sales, LLC Due to Their is a potential...

The Issue: Their is a potential that breast implants lack the lubricious coating that...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2024· Hologic, Inc

Recalled Item: BioZorb Marker-BioZorb 3D Bioabsorbable Marker-Intended Use radiographic...

The Issue: Safety Information: Complaints describe complications/adverse events that...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 13, 2024· Biomet, Inc.

Recalled Item: Vanguard Knee System AS Tibial Bearing / DCM ArCom Recalled by Biomet, Inc....

The Issue: Possible damage to the Vanguard Knee System AS Tibial Bearing caused during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2024· Electro Medical Systems SA

Recalled Item: Brand Name: WATER BOTTLE Product Name: WATER BOTTLE Model/Catalog Number:...

The Issue: Received complaints that bottles assembled with one batch of bottle collars...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2024· Electro Medical Systems SA

Recalled Item: Brand Name: PIEZON Bottle Product Name: PIEZON Bottle Model/Catalog Number:...

The Issue: Received complaints that bottles assembled with one batch of bottle collars...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2024· Electro Medical Systems SA

Recalled Item: Brand Name: CLEANER BOTTLE Product Name: CLEANER BOTTLE Model/Catalog...

The Issue: Received complaints that bottles assembled with one batch of bottle collars...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Iron3 - IVD use in the quantitative measurement Recalled by...

The Issue: Potential for falsely elevated Chol_2, LDLC, and Trig_2 results on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2024· Intuitive Surgical, Inc.

Recalled Item: Patient Cart Recalled by Intuitive Surgical, Inc. Due to Surgical system may...

The Issue: Surgical system may have inadequately welded top and/or bottom belts in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Achieva 3.0T Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: MR 7700 Recalled by Philips North America Llc Due to Patient support table...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: GYROSCAN T5 Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Intera Achieva 1.5T Pulsar Recalled by Philips North America Llc Due to...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Achieva 3.0TX for PET Recalled by Philips North America Llc Due to Patient...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Namic FLUID DELIVERY SET Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Products have a lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: namic CONVENIENCE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Products have a lack of sterility assurance.

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

Class II — Potential Health HazardOngoing