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. 2,503 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,503 in last 12 months

Showing 1162111640 of 27,512 recalls

Medical DeviceApril 30, 2020· Medtronic Inc.

Recalled Item: MiniMed 670G Recalled by Medtronic Inc. Due to Missing solder battery...

The Issue: Missing solder battery connection, which could interrupt power of insulin pump.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Medtronic Inc.

Recalled Item: MiniMed 640G Recalled by Medtronic Inc. Due to Missing solder battery...

The Issue: Missing solder battery connection, which could interrupt power of insulin pump.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Medtronic Inc.

Recalled Item: MiniMed 630G with SmartGuard Recalled by Medtronic Inc. Due to Missing...

The Issue: Missing solder battery connection, which could interrupt power of insulin pump.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Normand-Info S.A.S.U.

Recalled Item: Remisol Advance running Software Version 1.12 The Normand Info Remisol...

The Issue: Results from repeated run for WBC (White Bloodcell Count), UWBC (Urine Whit...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Elekta, Inc.

Recalled Item: Elekta Unity Recalled by Elekta, Inc. Due to potential risk that Legionella...

The Issue: potential risk that Legionella may be present in the Unity machine room,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Multi Display Manager in the Artis Systems (Image-Intensified Fluoroscopic...

The Issue: Artis systems containing a Multi Display Manager of a specific lot, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Hill-Rom, Inc.

Recalled Item: Centrella Smart+ Bed Recalled by Hill-Rom, Inc. Due to The Bed Exit System...

The Issue: The Bed Exit System may fail to send a remote alert through the nurse call...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Foley Catheter with Temperature...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Premium Urine Meter Foley Tray Recalled by Covidien Llc...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 400mL Recalled by Covidien Llc Due to Temperature sensing catheters...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 400 ml 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 400 ml 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Foley Catheter with Temperature...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Foley Catheter with Temperature 16FR 5CC2W Recalled by...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Foley Catheter with Temperature Sensor 14FR 5CC2W...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Premium Urine Meter Tray 400mL Recalled by Covidien Llc...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2020· GE Healthcare, LLC

Recalled Item: Giraffe Incubator with installed Servo Oxygen module. Infant incubator....

The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2020· GE Healthcare, LLC

Recalled Item: Giraffe OmniBed with installed Servo Oxygen module. Infant incubator and...

The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...

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

Class II — Potential Health HazardOngoing