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. 2,696 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,696 in last 12 months

Showing 91819200 of 28,744 recalls

Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: Outlook Pump Sets w/3 CARESITE Needle-Free Injection Sites: single-use for...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Smiths Medical ASD Inc.

Recalled Item: Bivona Aire-Cuf Endotracheal Tube Recalled by Smiths Medical ASD Inc. Due to...

The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Smiths Medical ASD Inc.

Recalled Item: Bivona Uncuffed Wire Endotracheal Tubes Recalled by Smiths Medical ASD Inc....

The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Beckman Coulter Inc.

Recalled Item: Access hsTnI High Sensitivity Troponin I Recalled by Beckman Coulter Inc....

The Issue: Through customer feedback, testing a sample with cardiac troponin I...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for Recalled...

The Issue: Incorrect version of labels were used.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the Recalled...

The Issue: Incorrect version of labels were used.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose Recalled...

The Issue: Incorrect version of labels were used.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· Johnson & Johnson Surgical Vision Inc

Recalled Item: TECNIS Eyhance IOLs are permanent intraocular implants intended for...

The Issue: Nonconforming product was distributed in error. Product was nonconforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll (SL-2593CO) Recalled by ZOLL Circulation, Inc. Due to Labeling update...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll (IC-3893CO) Recalled by ZOLL Circulation, Inc. Due to Labeling update...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing