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. 1,665 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,665 in last 12 months

Showing 4420144220 of 47,938 recalls

DrugMay 21, 2013· Fresenius Kabi USA, LLC

Recalled Item: Folic Acid Injection Recalled by Fresenius Kabi USA, LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specification

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

Class III — Low RiskOngoing
Refund
DrugMay 20, 2013· Dolphin Intertrade Corporation

Recalled Item: XIYOUJI QINGZHI CAPSULE Recalled by Dolphin Intertrade Corporation Due to...

The Issue: Marketed without an Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 20, 2013· Sandoz Incorporated

Recalled Item: Methotrexate Injection Recalled by Sandoz Incorporated Due to Presence of...

The Issue: Presence of Particulate Matter: Found during examination of retention samples.

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 20, 2013· Dolphin Intertrade Corporation

Recalled Item: JaDera Recalled by Dolphin Intertrade Corporation Due to Undeclared Sibutramine

The Issue: Marketed without an Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 20, 2013· Hospira, Inc.

Recalled Item: Ondansetron Injection Recalled by Hospira, Inc. Due to Presence of...

The Issue: Presence of Particulate; lot being recalled as a precaution due to the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 20, 2013· Olympus America Inc.

Recalled Item: Olympus Endoscopic Flushing Pump Recalled by Olympus America Inc. Due to...

The Issue: There is a possibility that the pump head was not shipped in the locked...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista(R) 500 and Dimension Vista(R) 1500 - Reloaded Vista Recalled...

The Issue: There is the potential for the vial volume of "in use" Vista calibrators,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2013· Steris Corporation

Recalled Item: STERIS Fine Traction Device Recalled by Steris Corporation Due to A bearing...

The Issue: A bearing used in the assembly of the Fine Traction Device did not perform...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2013· SpineFrontier, Inc.

Recalled Item: BASE Recalled by SpineFrontier, Inc. Due to The S-LIFT Instrument Case...

The Issue: The S-LIFT Instrument Case contained a bracket with peeling nylon coating.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2013· RF Technologies, Inc.

Recalled Item: Code Alert Advanced 4-Way Care Solution Recalled by RF Technologies, Inc....

The Issue: RF Technologies, Inc. has initiated a recall involving CA520 Code Alert...

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

Class II — Potential Health HazardOngoing
DrugMay 17, 2013· Warner Chilcott US LLC

Recalled Item: Enablex (darifenacin) Extended Release Tablet Recalled by Warner Chilcott US...

The Issue: Failed Impurities/Degradation Specifications: unspecified degradation product

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 17, 2013· Zip International Group LLC.

Recalled Item: Marmalade Fonariky Net 105.8 oz (3 kg) Product of Russia Recalled by Zip...

The Issue: Marmalade contains undeclared colors and dyes.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2013· Chs Inc

Recalled Item: Solcon S Functional Soy Protein Concentrates. Item No. / Item Recalled by...

The Issue: Certain Soy-based products produced at the Ashdod Israel production facility...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2013· Chs Inc

Recalled Item: Solcon Soy Protein Concentrates. Item No. / Item Description: 12110 Recalled...

The Issue: Certain Soy-based products produced at the Ashdod Israel production facility...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2013· Chs Inc

Recalled Item: Contex - Textured Soy Protein Concentrates Item No. / Item Recalled by Chs...

The Issue: Certain Soy-based products produced at the Ashdod Israel production facility...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 16, 2013· Chs Inc

Recalled Item: Solbar Q Soy Protein Isolates. Item No. / Item Description: Recalled by Chs...

The Issue: Certain Soy-based products produced at the Ashdod Israel production facility...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS System (HCP) The CoaguChek XS System is intended Recalled by...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS Pro System The CoaguChek XS Pro System (CoaguChek Recalled by...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS Plus System The CoaguChek XS Plus system for Recalled by Roche...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS System (PST) The CoaguChek XS PT test strips Recalled by Roche...

The Issue: Roche has confirmed the potential for an undetected elevated INR test result...

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

Class II — Potential Health HazardOngoing