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 4356143580 of 47,938 recalls

DrugJune 11, 2013· Bethel Nutritional Consulting, Inc

Recalled Item: Bethel 30 capsules Recalled by Bethel Nutritional Consulting, Inc Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 11, 2013· Church & Dwight Inc

Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...

The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 11, 2013· Church & Dwight Inc

Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...

The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 11, 2013· Philips Healthcare Inc.

Recalled Item: Philips Healthcare MobileDiagnostwDR system. Mobile Digital radiography...

The Issue: The Instructions for Use (IFU) for the MobileDiagnost wDR fails to comply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Flexible Medullary Reamer. Intended to be used to facilitate...

The Issue: Due to the coiled design for this product, the product is difficult to clean...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Dual Lumen Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Recalled by Integra...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Inegra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Dual Lumen Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· GE Healthcare It

Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...

The Issue: GE has recently become aware of potential issues due to out of context...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Recalled by Integra...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...

The Issue: Integra LifeSciences Corporation has determined that there is a possibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Radiometer America Inc

Recalled Item: pO2 D999 membrane units. Distributed by Radiometer America Recalled by...

The Issue: RADIOMETER became aware that the regarded lot pO2 units 942-042R0971 were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Biomet 3i, LLC

Recalled Item: Osseotite 2 Certain Prevail 5mm(D)X 4.1mm (P) X X 11.5mm Recalled by Biomet...

The Issue: One of the dental implants do not have the internal hex feature. One of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System UC Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing