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. 1,168 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
1,168 in last 12 months

Showing 2201–2220 of 52,482 recalls

Medical DeviceJune 23, 2025· Abiomed, Inc.

Recalled Item: Automated Impella Controller (AIC) Recalled by Abiomed, Inc. Due to A...

The Issue: A potential issue with the Automated Impella Controller (AIC) not detecting...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 23, 2025· Becton Dickinson & Co.

Recalled Item: BD COR System Software. Model Number: 444829. Recalled by Becton Dickinson &...

The Issue: Potential for functionality issue that supports the Over labeling feature...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2025· Covidien

Recalled Item: Covidien Nellcor Bedside SpO2 Patient Monitoring System: Recalled by...

The Issue: Bedside SpO2 Patient Monitoring System alarms not heard/recognized,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2025· GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING

Recalled Item: Varicam Recalled by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING Due to...

The Issue: Unintended radial detector motion may occur during patient setup or during...

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

Class II — Potential Health HazardOngoing
DrugJune 20, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...

The Issue: Subpotent Drug: Assay below the approved specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...

The Issue: Subpotent Drug: Assay below the approved specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...

The Issue: Subpotent Drug: Assay below the approved specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...

The Issue: Subpotent Drug: Assay below the approved specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...

The Issue: Subpotent Drug: Assay below the approved specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...

The Issue: Subpotent Drug: Assay below the approved specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2025· ACCORD HEALTHCARE, INC.

Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...

The Issue: Subpotent Drug: Assay below the approved specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2025· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg Recalled by Lupin...

The Issue: Product Mix Up: This product is being recalled because of a complaint...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2025· CinFranky LLC dba New Mexico Pinon Coffee

Recalled Item: New Mexico Pinon Coffee. Dark Pinon Single Serve 10ct. Product Recalled by...

The Issue: Clear coat seal on the lid of the single serve cups did not get applied...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceJune 20, 2025· GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING

Recalled Item: Infinia Recalled by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING Due to...

The Issue: Unintended radial detector motion may occur during patient setup or during...

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

Class II — Potential Health HazardOngoing
DrugJune 19, 2025· The Harvard Drug Group LLC

Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Defective...

The Issue: Defective container; blister packaging inadequately sealed.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2025· The Harvard Drug Group LLC

Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Defective...

The Issue: Defective container; blister packaging inadequately sealed.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 18, 2025· Medtronic, Inc.

Recalled Item: Medtronic CareLink SmartSync Patient Connector Recalled by Medtronic, Inc....

The Issue: In prior SmartSync application versions, the Abort button stopped the test...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2025· Osteotec Limited

Recalled Item: Brand Name: Osteotec Product Name: Osteotec Silicone Finger Implant...

The Issue: There is the potential that the silicone implant may contain foreign material

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

Class II — Potential Health HazardOngoing
FoodJune 18, 2025· Lipari Foods Operating Company, LLC.

Recalled Item: JLM Manufacturing Dark Chocolate Nonpareils Recalled by Lipari Foods...

The Issue: Undeclared milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 18, 2025· Stryker Corporation

Recalled Item: Stryker Recalled by Stryker Corporation Due to Due to complaints their is...

The Issue: Due to complaints their is the potential that irrigation solution may leaked...

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

Class II — Potential Health HazardOngoing