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. 2,466 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,466 in last 12 months

Showing 1578115800 of 27,512 recalls

Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid E9 ultrasound system Product Usage: GE Vivid E9 Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid 7 ultrasound system Product Usage: Vivid E7 is Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 Recalled...

The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE LOGIQ E9 ultrasound system Product Usage: The device is Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid E95 ultrasound system Product The device is intended Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ EDTA Pink Top Tube Recalled by Becton Dickinson & Company Due...

The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2018· Madison Polymeric Engineering

Recalled Item: First Step Endoscopic Cleaning Pad Recalled by Madison Polymeric Engineering...

The Issue: The products exhibit an unpleasant odor due to microbial contamination with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Madison Polymeric Engineering

Recalled Item: Draco Enzymatic Deep-Cleaning Pad Recalled by Madison Polymeric Engineering...

The Issue: The products exhibit an unpleasant odor due to microbial contamination with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Madison Polymeric Engineering

Recalled Item: First Step Endoscopic Cleaning Pad Recalled by Madison Polymeric Engineering...

The Issue: The products exhibit an unpleasant odor due to microbial contamination with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Madison Polymeric Engineering

Recalled Item: First Step Endoscopic Cleaning Pad Recalled by Madison Polymeric Engineering...

The Issue: The products exhibit an unpleasant odor due to microbial contamination with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ CTNI Sample Diluent Recalled by Siemens Healthcare...

The Issue: The diluent may have an incomplete slit on the septum in the cap of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ MULTI 1 SDIL Recalled by Siemens Healthcare Diagnostics,...

The Issue: The diluent may have an incomplete slit on the septum in the cap of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Madison Polymeric Engineering

Recalled Item: First Step Endoscopic Cleaning Pad with 4" Button Brush Recalled by Madison...

The Issue: The products exhibit an unpleasant odor due to microbial contamination with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Madison Polymeric Engineering

Recalled Item: Travel Kit Recalled by Madison Polymeric Engineering Due to The products...

The Issue: The products exhibit an unpleasant odor due to microbial contamination with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ MULTI 2 SDIL Recalled by Siemens Healthcare Diagnostics,...

The Issue: The diluent may have an incomplete slit on the septum in the cap of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Ultra TouchTM Push Button Blood Collection Set 0.6 Recalled...

The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set 0.6 x 19 Recalled by Becton...

The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2018· Certified Safety Mfg Inc

Recalled Item: First aid/emergency kits containing Honeywell eyewash: CSM kit number...

The Issue: Firm is recalling first aid/emergency kits and cabinets which contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set 0.8 x 19 Recalled by Becton...

The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2018· Synthes, Inc.

Recalled Item: Stem Extractor f/Guide Bar Recalled by Synthes, Inc. Due to There is a...

The Issue: There is a potential for the connection screw of the stem extractor to break.

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

Class II — Potential Health HazardOngoing