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. 2,510 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,510 in last 12 months

Showing 1070110720 of 27,512 recalls

Medical DeviceOctober 22, 2020· Cook Inc.

Recalled Item: Fixed Core Wire Guide Recalled by Cook Inc. Due to Affected product was...

The Issue: Affected product was dropped during manufacturing, which may result in a...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to Some...

The Issue: Some electronic components within the generator were equipped with an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2020· Viewray, Inc.

Recalled Item: ViewRay MRIdian System: Model No. 10000 Recalled by Viewray, Inc. Due to...

The Issue: There is a potential that components of the receive coil can reach elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2020· Viewray, Inc.

Recalled Item: ViewRay MRIdian Linac System: Model No. 20000 Recalled by Viewray, Inc. Due...

The Issue: There is a potential that components of the receive coil can reach elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2020· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250i Recalled by Mevion Medical Systems, Inc. Due to Treatment beam...

The Issue: Treatment beam information disappears on Treatment Console screen while beam...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2020· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen 0.25-1mm 0.25g - Product Usage: natural bone Recalled...

The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2020· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen 1-2mm 0.5g - Product Usage: natural bone Recalled by...

The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2020· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen 0.25-1mm 0.5g - Product Usage: natural bone Recalled...

The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Chemistry Products Performance Verifier II-For in vitro diagnostic...

The Issue: Product instability; biased ALKP values obtained from VITROS Chemistry...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2020· Covidien Llc

Recalled Item: Puritan Bennett 980 (PB980) Ventilator Series - Product Usage: for Recalled...

The Issue: In-house lab observations and customer reports of overheating and/or thermal...

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

Class II — Potential Health HazardOngoing