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. 2,448 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,448 in last 12 months

Showing 1726117280 of 27,512 recalls

Medical DeviceMay 23, 2017· Shimadzu Medical Systems Usa Com

Recalled Item: SHIMADZU RADspeed Pro Catalog Number: RADspeed Pro Recalled by Shimadzu...

The Issue: Cracks may occur over time on the tube holding shaft near the base of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Magellan Diagnostics, Inc.

Recalled Item: Magellan Diagnostics LeadCare Ultra and LeadCare Plus test Kits. Product...

The Issue: Underestimates the lead concentration of venous blood samples when the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 23, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Protein 1 Control M Recalled by Siemens Healthcare...

The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Shimadzu Medical Systems Usa Com

Recalled Item: SHIMADZU Ceiling Type X-ray Tube Support CH-200/CH-200M Catalog Number:...

The Issue: Cracks may occur over time on the tube holding shaft near the base of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Shimadzu Medical Systems Usa Com

Recalled Item: SHIMADZU FDR Visionary Catalog Number: FDR Visionary Suite Stationary x-ray...

The Issue: Cracks may occur over time on the tube holding shaft near the base of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Magellan Diagnostics, Inc.

Recalled Item: Magellan Diagnostics LeadCare and LeadCare II test Kits. Product Usage:...

The Issue: Underestimates the lead concentration of venous blood samples when the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 23, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Protein 1 Control H Recalled by Siemens Healthcare...

The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Zimmer Periarticular Locking Plate System Drill Standard 2.7 mm Diameter...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Flowonix Medical, Inc.

Recalled Item: PROMETRA II Programmable Infusion Pump Recalled by Flowonix Medical, Inc....

The Issue: Flowonix Medical received a report of a patient implanted with the Prometra...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Natus Medical Incorporated

Recalled Item: The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended...

The Issue: Olympic Pasteurmatic 3000/3500 Systems are recalled because they do not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Zimmer Periarticular Locking Plate System Locking Screw Tap Standard...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: ECT Internal Fracture Fixation Drill Bits 3.2 mm Diameter (.126 Inch)...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail System Freehand Drill 4.3 mm Diameter 152.5 mm Length...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: ECT Internal Fracture Fixation Drill 1.5 mm Diameter (.059 Inch) Recalled by...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Drill Bit Quick-Connect 1.5 mm Diameter 85 mm Length Recalled by Zimmer...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Drill Bit Quick-Connect 3.2 mm Diameter 195 mm Length Recalled by Zimmer...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: ECT Internal Fracture Fixation Drill 1.1 mm Diameter (.043 Inch) Recalled by...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Zimmer Trabecular Metal Reverse Shoulder System Instrumentation Recalled by...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: M/DN Intramedullary Fixation Femoral Drill Large 5.0 mm Item Number/EDI...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: ECT Internal Fracture Fixation Quick-Connect Drill 2.0 mm Diameter 12.5...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing