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. 1,897 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
1,897 in last 12 months

Showing 2882128840 of 52,482 recalls

Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Arrow Multi Lumen CVC Kit (Central venous catheter) Recalled by Arrow...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi Lumen Central Venous Catheterization Kit with Blue...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Plus Multi Lumen CVC (Central venous catheter) Recalled by...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Multi Lumen Central Venous Catheterization Kit Recalled by Arrow...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Central Venous Catheterization Kit with Blue FlexTip Catheter Recalled by...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: AGB+ Multi Lumen Central Venous Catheterization Kit Recalled by Arrow...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS MultiLumen Central Venous...

The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2017· Fukuda Denshi Co., Ltd.

Recalled Item: Fukuda Denshi patient monitor model DS-8100M and DS-8100N Product Usage:...

The Issue: For the Fukuda Denshi patient monitor model DS-8100, in less than 0.003%...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2017· DeRoyal Industries Inc

Recalled Item: DeRoyal Sterile Custom kits containing Medline Aplicare Povidone Iodine Prep...

The Issue: Custom surgical kits contain Aplicare Povidone Iodine Prep Pads which were...

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

Class II — Potential Health HazardOngoing
DrugOctober 13, 2017· Sanofi-Aventis U.S. LLC

Recalled Item: Clofarabine injection Recalled by Sanofi-Aventis U.S. LLC Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Package Insert: authorized generic product...

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

Class III — Low RiskOngoing
Refund
FoodOctober 13, 2017· San Gennaro Foods, Inc

Recalled Item: Traditional Polenta Recalled by San Gennaro Foods, Inc Due to Date coding...

The Issue: Date coding ink was being printed directly on the food contact surface of...

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

Class III — Low RiskOngoing
Refund
FoodOctober 13, 2017· San Gennaro Foods, Inc

Recalled Item: Sun-Dried Tomato Polenta Recalled by San Gennaro Foods, Inc Due to Date...

The Issue: Date coding ink was being printed directly on the food contact surface of...

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

Class III — Low RiskOngoing
Refund
FoodOctober 13, 2017· San Gennaro Foods, Inc

Recalled Item: Red & Black Quinoa Organic Polenta Recalled by San Gennaro Foods, Inc Due to...

The Issue: Date coding ink was being printed directly on the food contact surface of...

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

Class III — Low RiskOngoing
Refund
FoodOctober 13, 2017· San Gennaro Foods, Inc

Recalled Item: Italian Herb Polenta Recalled by San Gennaro Foods, Inc Due to Date coding...

The Issue: Date coding ink was being printed directly on the food contact surface of...

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

Class III — Low RiskOngoing
Refund
FoodOctober 13, 2017· San Gennaro Foods, Inc

Recalled Item: Mushroom and Onion Organic Polenta Recalled by San Gennaro Foods, Inc Due to...

The Issue: Date coding ink was being printed directly on the food contact surface of...

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

Class III — Low RiskOngoing
Refund