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. 2,363 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,363 in last 12 months

Showing 2696126980 of 27,512 recalls

Medical DeviceMay 11, 2012· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 151F7. For...

The Issue: The device is being recalled because the firm received multiple complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Vygon VY(TM)Flush Heparin Lock Flush Syringes Recalled by Vygon Corporation...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 141F7. For...

The Issue: The device is being recalled because the firm received multiple complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131HF7P....

The Issue: The device is being recalled because the firm received multiple complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Vygon Corporation

Recalled Item: Churchill Medical Systems Recalled by Vygon Corporation Due to Manufacturer...

The Issue: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 volume imaging ultrasound systems at software versions VA16C...

The Issue: In some cases, the system is unable to capture a clip or image during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: CPB CATHETER KIT- DR OWEN Product Usage: The Sarns Cardioplegia Recalled by...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· RAYSEARCH LABORATORIES AB

Recalled Item: Brand name: RayStation. Generic name: Treatment Planning System. Software...

The Issue: The firm decided to recall when an issue was found with the dose calculation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Antegrade Cardioplegia Cannula: ROOT INFUSTION VENT CATHETER WITH 12...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: X-COATED TRANSPLANT PACK Product Usage: The Sarns Cardioplegia Cannula and...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: FX PACK Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: SARNS ANTEGRADE CARDIOPLEGIA CANNULA: ROOT INFUSION CANNULA WITH 12-GAUGE...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: INDIANA/OHIO HEART Product Usage: The Sarns Cardioplegia Cannula and...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: CPB CATHETER KIT-DR VANTRIGHT Product Usage: The Sarns Cardioplegia Cannula...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: SARNS ANTEGRADE CARDIOPLEGIA CANNULA: ROOT INFUSION CANNULA WITH 14-GAUGE...

The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...

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

Class II — Potential Health HazardOngoing