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 4422144240 of 47,938 recalls

Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Unitized BactiSeal...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Siphonguard Recalled by...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve only with SiphonGuard...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Catheter and Recalled by...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve Only Product Code: Recalled...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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 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
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 (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
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Theraflu Nighttime Warming Relief Nighttime Multi-Symptom Cold Recalled by...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Day/Night Cold & Cough Recalled by Novartis...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Excedrin Recalled by Novartis Consumer Health Due to Failed...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Theraflu Warming Relief Recalled by Novartis Consumer Health Due to Failed...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Nighttime Cold & Cough Recalled by Novartis...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Recalled by Novartis Consumer Health Due to Failed...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Recalled by Novartis Consumer Health Due to Failed...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Actavis South Atlantic LLC

Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution USP) 15 mg/mL Recalled by Actavis...

The Issue: Failed Impurity/Degradation Specification; "Related Compound C"

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 15, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Budesonide Capsules Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Dissolution Specifications: Routine stability testing at the 12-month...

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

Class III — Low RiskOngoing
Refund