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 2221–2240 of 52,482 recalls

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
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
FoodJune 18, 2025· Prestige Brands Holdings

Recalled Item: Little Remedies¿ Honey Cough 4 FL OZ (118 mL) Recalled by Prestige Brands...

The Issue: contaminated with Bacillus cereus and may be spoiled

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

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

Recalled Item: Medtronic CareLink SmartSync Device Manager Recalled by Medtronic, Inc. Due...

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
FoodJune 18, 2025· Krasnyi Oktyabr USA Inc

Recalled Item: ARAL FISH Recalled by Krasnyi Oktyabr USA Inc Due to Clostridium botulinum...

The Issue: Clostridium botulinum (uneviscerated fish)

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 18, 2025· Professional Botanicals, Inc.

Recalled Item: Product Name: Nutra Calm Package: 175cc HDPE Bottle. Type: Vegetable...

The Issue: Products contains Magnesium Salicylate.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2025· Professional Botanicals, Inc.

Recalled Item: Product Name: Tense-X. Package: 175cc HDPE Bottle. Type: Vegetable Capsule....

The Issue: Products contains Magnesium Salicylate.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2025· Professional Botanicals, Inc.

Recalled Item: Product Name: Total Comfort. Package: 175cc HDPE Bottle. Type: Vegetable...

The Issue: Products contains Magnesium Salicylate.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 17, 2025· Quidel Corporation

Recalled Item: QuickVue: Dipstick Strep A Test: 50T Recalled by Quidel Corporation Due to...

The Issue: Dipstick strep A test has potential for false positive results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2025· CARIS LIFE SCIENCES

Recalled Item: MI Cancer Seek UDI Code: (01)00860008613325(21)H5HJHDSXF MI Cancer Recalled...

The Issue: Due to an incorrect test results provided that indicated the incorrect drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2025· Draeger, Inc.

Recalled Item: SafeStar 55 Plus Filter. Bidirectionally breathing system filter. Recalled...

The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2025· CooperVision, Inc.

Recalled Item: Biofinity XR Toric Contact Lens Recalled by CooperVision, Inc. Due to Lens...

The Issue: Lens blisters may have an incomplete or leaking seal which may render them...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2025· BD SWITZERLAND SARL

Recalled Item: BD PhaSeal Injector Luer (N30C) Recalled by BD SWITZERLAND SARL Due to...

The Issue: Closed system drug transfer devices were shipped to the U.S. market without...

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

Class II — Potential Health HazardOngoing
DrugJune 16, 2025· B BRAUN MEDICAL INC

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B BRAUN MEDICAL INC Due to...

The Issue: Lack of assurance of sterility: pinholes, within the finger boxes used...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 16, 2025· Draeger, Inc.

Recalled Item: SafeStar 60A Plus Filter. Bidirectionally breathing system filter. Recalled...

The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...

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

Class I — Serious Health HazardOngoing
DrugJune 16, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: An out of specification results observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 16, 2025· Qualgen, LLC

Recalled Item: Testosterone 200 mg Pellet packaged in 1mL amber vials Recalled by Qualgen,...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date: A printing issue...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 16, 2025· CooperVision, Inc.

Recalled Item: Biofinity Toric Multifocal Contact Lens Recalled by CooperVision, Inc. Due...

The Issue: Lens blisters may have an incomplete or leaking seal which may render them...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2025· Draeger, Inc.

Recalled Item: SafeStar 90 Plus Filter. Bidirectionally breathing system filter. Recalled...

The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2025· Draeger, Inc.

Recalled Item: HME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter....

The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...

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

Class I — Serious Health HazardOngoing