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 81418160 of 52,482 recalls

Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· EITAN MEDICAL LTD

Recalled Item: Sapphire Infusion Pumps Recalled by EITAN MEDICAL LTD Due to Infusion Pumps...

The Issue: Infusion Pumps with affected software revision may fail to detect air in...

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

Class I — Serious Health HazardOngoing
FoodSeptember 9, 2023· Lipari Foods Operating Company, LLC.

Recalled Item: IO Inspired Organics Organic Raw Walnuts Recalled by Lipari Foods Operating...

The Issue: Undeclared cashews

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 8, 2023· Church & Dwight Inc

Recalled Item: TheraBreath for Kids! Oral Rinse Recalled by Church & Dwight Inc Due to...

The Issue: Microbial contamination of Non-Sterile Product; presence of yeast identified...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 8, 2023· Novartis Pharmaceuticals Corp.

Recalled Item: SANDIMMUNE Oral Solution (cyclosporine oral solution Recalled by Novartis...

The Issue: Crystallization: bottles of Sandimmune Oral Solution were determined to...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 8, 2023· GE Healthcare

Recalled Item: Universal Viewer Workflow Manager Recalled by GE Healthcare Due to When...

The Issue: When using Universal Viewer or Centricity Universal Viewer with Workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2023· GE Healthcare

Recalled Item: Centricity Universal Viewer Workflow Manager Recalled by GE Healthcare Due...

The Issue: When using Universal Viewer or Centricity Universal Viewer with Workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2023· GE Medical Systems China Co., Ltd.

Recalled Item: F2-01 Frame Recalled by GE Medical Systems China Co., Ltd. Due to There is a...

The Issue: There is a potential interruption of data communication between E-modules...

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

Class II — Potential Health HazardOngoing
DrugSeptember 7, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Cequa (cyclosporine ophthalmic solution) 0.09% Recalled by SUN...

The Issue: Subpotent: Out of Specification result observed for low assay

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 7, 2023· Blue Belt Technologies, Inc

Recalled Item: Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software...

The Issue: CORI software was missing a planning stage that appears in cases of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Beckman Coulter Biomedical Division

Recalled Item: AU/DxC AU Chemistry Transferrin Immune complexes formed in Recalled by...

The Issue: The firm has identified that the Transferrin reagent does not meet the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Modena-IVD Clinical Chemistry Analyser Catalog Number: RX9000 Recalled by...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Monaco-IVD Clinical Chemistry Analyser Catalog Number: RX5000 Recalled by...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Imola-IVD Clinical Chemistry Analyzer Catalog Number: RX4900. RX4900R ()...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Daytona Plus (with ISE)-IVD Clinical Chemistry Analyser Catalog Number:...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Daytona Plus (without ISE)- IVD Clinical Chemistry Analyser (1) RX4041...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T HD SYS. W/O CDX BLUESTAR Recalled by Fresenius Medical Care Holdings,...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T Hemodialysis SYS Recalled by Fresenius Medical Care Holdings, Inc. Due...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T HD SYS. W/O CDX W/BIBAG BLUESTAR Recalled by Fresenius Medical Care...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T Hemodialysis System w/Bibag Recalled by Fresenius Medical Care...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing