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. 2,573 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,573 in last 12 months

Showing 20412060 of 47,938 recalls

Medical DeviceJune 25, 2025· Beckman Coulter, Inc.

Recalled Item: DxI 600 Access Immunoassay Analyzer W/Spot B Recalled by Beckman Coulter,...

The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2025· Beckman Coulter, Inc.

Recalled Item: DxI 800 Access Immunoassay Analyzer W/Spot B Recalled by Beckman Coulter,...

The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2025· Beckman Coulter, Inc.

Recalled Item: DxI 600 Access Immunoassay Analyzer W/Dual Gantry Recalled by Beckman...

The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2025· Beckman Coulter, Inc.

Recalled Item: UniCel DxI 600 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc....

The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2025· Beckman Coulter, Inc.

Recalled Item: UniCel DxI 800 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc....

The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...

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

Class II — Potential Health HazardOngoing
FoodJune 24, 2025· Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Recalled Item: Lithium Orotate Recalled by Enjoy Nutrition, LLC; dba Weyland Brain...

The Issue: Under potency / misbranding: product fails to meet labeled lithium orotate...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodJune 24, 2025· Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Recalled Item: Lithium Orotate Recalled by Enjoy Nutrition, LLC; dba Weyland Brain...

The Issue: Under potency / misbranding: product fails to meet labeled lithium orotate...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodJune 24, 2025· Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Recalled Item: Lithium Orotate Recalled by Enjoy Nutrition, LLC; dba Weyland Brain...

The Issue: Under potency / misbranding: product fails to meet labeled lithium orotate...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodJune 24, 2025· Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Recalled Item: Lithium Orotate Recalled by Enjoy Nutrition, LLC; dba Weyland Brain...

The Issue: Under potency / misbranding: product fails to meet labeled lithium orotate...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodJune 24, 2025· Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Recalled Item: Lithium Orotate Recalled by Enjoy Nutrition, LLC; dba Weyland Brain...

The Issue: Under potency / misbranding: product fails to meet labeled lithium orotate...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
DrugJune 24, 2025· Granules Pharmaceuticals Inc.

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Granules...

The Issue: Failed Dissolution Specifications: Product failed to meet dissolution...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 24, 2025· Fresenius Kabi USA, LLC

Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Potential for external cassette leaks

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2025· Fresenius Kabi USA, LLC

Recalled Item: LVP Blood Products Administration Set Dual-Inlet Recalled by Fresenius Kabi...

The Issue: Potential for external cassette leaks

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2025· Orthofix U.S. LLC

Recalled Item: PILLAR SA Ti Recalled by Orthofix U.S. LLC Due to A 37 mm implant width...

The Issue: A 37 mm implant width intervertebral body fusion device has a labeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2025· Fresenius Kabi USA, LLC

Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Potential for external cassette leaks

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2025· Fresenius Kabi USA, LLC

Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Potential for external cassette leaks

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2025· Preat Corp

Recalled Item: Preat Recalled by Preat Corp Due to Due to manufacturing error, digital...

The Issue: Due to manufacturing error, digital analog rotational feature is 180 degrees...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2025· Thoratec LLC

Recalled Item: Brand Name: HeartMate Product Name: Mobile Power Unit Recalled by Thoratec...

The Issue: Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 23, 2025· Thoratec LLC

Recalled Item: Brand Name: HeartMate Product Name: Mobile Power Unit Model/Catalog Number:...

The Issue: Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 23, 2025· Abiomed, Inc.

Recalled Item: Automated Impella Controller (AIC) Recalled by Abiomed, Inc. Due to A...

The Issue: A potential issue with the Automated Impella Controller (AIC) not detecting...

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

Class I — Serious Health HazardOngoing