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. 925 recalls have been distributed to North Dakota in the last 12 months.
Showing 41561–41580 of 47,938 recalls
Recalled Item: CSI Recalled by Cardiovascular Systems, Inc. Due to Cardio vascular Systems...
The Issue: Cardio vascular Systems Inc. has initiated a recall to request the immediate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 3.2 mm Guide Wire 400mm. Used for guiding the Recalled by Synthes,...
The Issue: Synthes 3.2 mm Guide Wire 400mm included an incorrect raw material listed on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Dynamics Picture Archiving and Communication System (PACS). Model...
The Issue: Potential patient data mixup. Improper error handling could allow for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Notch Titanium Reconstructive Plate Product Usage: The Synthes...
The Issue: Certain modules containing the Synthes Small Notch Titanium Reconstructive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suprax Recalled by Lupin Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product did not meet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Suprax Recalled by Lupin Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product did not meet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pringles Recalled by Kellogg Company Due to Undeclared Milk
The Issue: Undeclared milk, an allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RetCam 3 Recalled by Clarity Medical Systems Inc Due to Software anomaly for...
The Issue: Software anomaly for RetCam 3, RetCam Shuttle and RetCam Portable with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaSure Impedance Controlled Endometrial Ablation System Radiofrequency...
The Issue: NovaSure Radiofrequency Control Units may not meet a requirement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeCare 5000 Pump (Plum 1.6) infusion pump Recalled by Hospira Inc. Due to...
The Issue: There is the potential for the door roller assembly on the Plum LifeCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum XL3 Multi line Infusion System Recalled by Hospira Inc. Due to There is...
The Issue: There is the potential for the door roller assembly on the Plum LifeCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum XL Recalled by Hospira Inc. Due to There is the potential for the door...
The Issue: There is the potential for the door roller assembly on the Plum LifeCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Kodak 2100 Intraoral X-Ray System Recalled by Carestream Health Inc....
The Issue: Carestream received problem reports relating to apparent early failure of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model: 861290 The HeartStart...
The Issue: HeartStart XL+ battery charge time to 100% capacity at 35¿C (95¿F) is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Kodak 2200 Intraoral X-Ray System Recalled by Carestream Health Inc....
The Issue: Carestream received problem reports relating to apparent early failure of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JIANFEIJINDAN Activity Girl Capsules Recalled by MyNicNaxs, Inc. Due to...
The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SlimEasy Herbs Capsule Recalled by MyNicNaxs, Inc. Due to Undeclared Active
The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Teva Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due...
The Issue: CGMP Deviations: Dextroamphetamine Saccharate, Amphetamine Asparate,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pill for weight reduction Recalled by MyNicNaxs, Inc. Due to Undeclared Active
The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Super Fat Burning Bomb Capsules Recalled by MyNicNaxs, Inc. Due to...
The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.