Product Recalls in North Dakota

Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 902 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
902 in last 12 months

Showing 47341–47360 of 47,938 recalls

DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugMay 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution Recalled by Guthy-Renker LLC Due to...

The Issue: Subpotent Drug: Salicylic acid is subpotent.

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 4, 2012· Stanley Security Solutions, Inc.

Recalled Item: Tabs Professional Monitor Recalled by Stanley Security Solutions, Inc. Due...

The Issue: The monitor may fail to sound an alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· Stanley Security Solutions, Inc.

Recalled Item: Tabs Professional Monitor Recalled by Stanley Security Solutions, Inc. Due...

The Issue: The monitor may fail to sound an alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· Stanley Security Solutions, Inc.

Recalled Item: Tabs Professional Voice + Monitor Recalled by Stanley Security Solutions,...

The Issue: The monitor may fail to sound an alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· Stanley Security Solutions, Inc.

Recalled Item: Tabs Professional Voice + Monitor Recalled by Stanley Security Solutions,...

The Issue: The monitor may fail to sound an alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· Stanley Security Solutions, Inc.

Recalled Item: Tabs Professional Monitor Recalled by Stanley Security Solutions, Inc. Due...

The Issue: The monitor may fail to sound an alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Scenaria CT System Software Product Usage: The Scenaria system...

The Issue: Hitachi discovered a software error in the Reconstruction Status function...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Depuy Spine Side Fire Needles 11G X 6IN Side-Fire Needle Recalled by DePuy...

The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Depuy Spine Side Fire Needles 13G X 6IN Recalled by DePuy Mitek, Inc., a...

The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Depuy Spine Side Fire Needles 11G X 4IN Recalled by DePuy Mitek, Inc., a...

The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Depuy Spine Side Fire Needles 13G X 4IN Side-Fire Needle Recalled by DePuy...

The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...

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

Class II — Potential Health HazardOngoing
FoodMay 4, 2012· FunFresh Foods Inc

Recalled Item: FunFresh Foods World Berry Organic Cacao Nibs 6 oz Recalled by FunFresh...

The Issue: FunFresh Foods World Berry Cacao Nibs 6 oz snack food contaminated with E. coli.

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

Class III — Low RiskOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 5% Dextrose and 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 1.5% Glycine Irrigation Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 4, 2012· Hospira Inc.

Recalled Item: 70% Dextrose Injection USP Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the...

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

Class II — Potential Health HazardOngoing
Refund