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 48214840 of 52,482 recalls

Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 with SmartAssist S2 Set Recalled by Abiomed, Inc. Due to A...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 with SmartAssist Set Recalled by Abiomed, Inc. Due to A...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Pump Set Recalled by Abiomed, Inc. Due to A potential device...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Pump 371 14F LT CMR Set Recalled by Abiomed, Inc. Due to A potential device...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 Set AU Recalled by Abiomed, Inc. Due to A potential device...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 with SmartAssist Set Recalled by Abiomed, Inc. Due to A...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
DrugAugust 2, 2024· EMPOWER CLINIC SERVICES LLC

Recalled Item: Empower Pharmacy Recalled by EMPOWER CLINIC SERVICES LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 2, 2024· AURIS HEALTH INC

Recalled Item: Monarch Platform (Endoscopy) Recalled by AURIS HEALTH INC Due to...

The Issue: Endoscopy/bronchoscopy/urology devices may have a strain relief defect with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2024· AURIS HEALTH INC

Recalled Item: Monarch Platform (Urology) Recalled by AURIS HEALTH INC Due to...

The Issue: Endoscopy/bronchoscopy/urology devices may have a strain relief defect with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2024· Bard Peripheral Vascular Inc

Recalled Item: BARD MAGNUM Disposable Core Tissue Biopsy Needle MN Recalled by Bard...

The Issue: Due to possible packaging damage (indentations/cuts) cause by manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2024· Ultradent Products, Inc.

Recalled Item: Brand Name: Transcend Product Name: Transcend Singles Universal Body (UB)...

The Issue: Due to a manufacturing issue, red particulates present in the expressed...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2024· Ultradent Products, Inc.

Recalled Item: Brand Name: Transcend Product Name: Transcend Econo Kit (UB) - Recalled by...

The Issue: Due to a manufacturing issue, red particulates present in the expressed...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2024· Ultradent Products, Inc.

Recalled Item: Brand Name: Vit-l-escence Product Name: Vit-l-escence Singles A3...

The Issue: Due to a manufacturing issue, red particulates present in the expressed...

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

Class II — Potential Health HazardOngoing
DrugAugust 1, 2024· Baxter Healthcare Corporation

Recalled Item: Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection) Recalled by...

The Issue: Microbial Contamination of Sterile Products; out of limit results obtained...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugAugust 1, 2024· Amneal Pharmaceuticals, LLC

Recalled Item: Methotrexate Tablets Recalled by Amneal Pharmaceuticals, LLC Due to Presence...

The Issue: Presence of Foreign Tablets: Potential presence of Fludrocortisone Acetate...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 1, 2024· Outset Medical, Inc.

Recalled Item: Tablo Console Recalled by Outset Medical, Inc. Due to Blood leak sensor, a...

The Issue: Blood leak sensor, a component of hemodialysis device, may show decreased...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX FC ESO STENT RMV LL 18X103- Wallflex Esophageal Partially Recalled...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing