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. 1,672 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,672 in last 12 months

Showing 4198142000 of 47,938 recalls

Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Comfort Infusion Set with 60cm tubing & 17mm cannula packaged in...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Comfort Infusion Set with 110cm tubing & 17mm cannula Recalled by...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Conset Infusion Set with 60cm tubing & 9mm cannula packaged in...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution CR Articular Surface Provisional-Purple 9mm...

The Issue: This is an expansion of the June 2013 recall of NexGen Micro components....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Oasis Dry Suction Water Seal ATS (Autotransfusion) Blood Recovery...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution CR Articular Surface Provisional-Striped Green...

The Issue: This is an expansion of the June 2013 recall of NexGen Micro components....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Ocean Water Seal Chest Drain ATS Blood Recovery System Recalled by...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Comfort Infusion Set with 110cm tubing & 13mm cannula packaged in...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Ultradent Products, Inc.

Recalled Item: Opal Orthodontics by Ultradent. Avex CX2 Ceramic Orthodontic Brackets Avex...

The Issue: Ultradent Products Inc. is recalling various lots of Avex CX2 Orthodontic...

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

Class III — Low RiskOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Conset Infusion Set with tubing & 9mm cannula packaged in 5-packs...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Express Dry Seal ATS (Autotransfusion) Blood Recovery System Chest...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Conset Infusion Set with 60cm tubing & 6mm cannula packaged in...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
DrugNovember 19, 2013· Tendex

Recalled Item: NATURECT Capsules Dietary Supplement 500 mg Recalled by Tendex Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 19, 2013· Tendex

Recalled Item: P-BOOST Capsules Dietary Supplement 500 mg Recalled by Tendex Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 19, 2013· Vitality Research Labs LLC

Recalled Item: vitaliKOR Ready When You Are Recalled by Vitality Research Labs LLC Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling found undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Baxter Healthcare Corp.

Recalled Item: Clinimix 5/15 sulfite-free (5% Amino Acid in 15% Dextrose) Injection...

The Issue: Presence of Particulate Matter: Particulate matter includes wood, sodium...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Baxter Healthcare Corp.

Recalled Item: 50 mg Nitroglycerin in 5% Dextrose Injection (200 mcg/mL) Recalled by Baxter...

The Issue: Presence of Particulate Matter; particulate matter in one vial identified as...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Fossil Fuel Products, LLC

Recalled Item: RezzRX capsules Recalled by Fossil Fuel Products, LLC Due to Undeclared...

The Issue: Marketed Without an Approved NDA/ANDA: Fossil Fuel Products, is recalling...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Baxter Healthcare Corp.

Recalled Item: Clinimix E 4.25/10 sulfite-free (4.25% Amino Acid with Electrolytes in...

The Issue: Presence of Particulate Matter: Particulate matter includes wood, sodium...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Baxter Healthcare Corp.

Recalled Item: Clinimix 4.25/25 sulfite-free (4.25% Amino Acid in 25% Dextrose) Injection...

The Issue: Presence of Particulate Matter: Particulate matter includes wood, sodium...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund