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. 1,917 recalls have been distributed to Wisconsin in the last 12 months.
Showing 26921–26940 of 52,482 recalls
Recalled Item: Baskin Robbins Mint Chocolate Chip Recalled by Dean Foods, Inc. Due to...
The Issue: Product may contain unlabeled coconut.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Acne Shave Post-Shave Moisturizer (salicylic acid) Recalled by Shadow...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acne Shave 3 Step Shaving System Recalled by Shadow Holdings DBA Bocchi Labs...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acne Shave (salicylic acid) Shave Cream Acne Shield Recalled by Shadow...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: X-Jow (menthol USP) Pain Gel Recalled by Shadow Holdings DBA Bocchi Labs Due...
The Issue: CGMP Deviations: products may be contaminated with bacteria.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artis zee systems with Laird Cooling Unit for SSFD: Material Recalled by...
The Issue: Due to a defective sealing, coolant may inflow into the electrical parts of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis with Laird Cooling Unit for SSFD: Material # Recalled by Siemens...
The Issue: Due to a defective sealing, coolant may inflow into the electrical parts of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM/CT 670 ES Recalled by GE Healthcare, LLC Due to When your...
The Issue: When your system was installed, the Main disconnect switch, EPO button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perseus A500 Anesthesia Machine Recalled by Draeger Medical, Inc. Due to The...
The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius GS MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due to...
The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CT Goldseal Optima CT 600 Recalled by GE Healthcare, LLC Due to Some CT and...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Two...
The Issue: Two lots of tibial bearings were commingled. There is a possibility that a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius GS Premium Anesthesia Machine Recalled by Draeger Medical, Inc. Due...
The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution EVO 3.6 Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius GS Tiro Anesthesia Machine Recalled by Draeger Medical, Inc. Due to...
The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorting-Drive Professional Part Recalled by Beckman Coulter Inc. Due to...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intelligent Peri-Analytical Workstation (HW+SW) Recalled by Beckman Coulter...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.