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. 1,826 recalls have been distributed to North Dakota in the last 12 months.
Showing 23861–23880 of 47,938 recalls
Recalled Item: Amlodipine Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine and Valsartan Tablets Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EEA Circular Stapler with Tri-Staple Technology Recalled by COVIDIEN LLC Due...
The Issue: The firm identified the potential for a device to have an incorrect tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Montelukast Sodium Tablets 10 mg Recalled by Hetero Labs Limited Unit V Due...
The Issue: Labeling: Label Mix-Up - One lot labeled Montelukast Sodium Tablets 10 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TriMed Olecranon Hook Plate Recalled by TriMed Inc. Due to The firm has...
The Issue: The firm has become aware that the angled-hole of certain semi-tubular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MassHunter Quantitative Analysis Software Recalled by Agilent Technologies,...
The Issue: When utilizing specific software versions of an LC/MS device, and Batch at a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System- (). For use in the in Recalled by...
The Issue: Potential for the VITROS 5600 Integrated System to dispense an insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System-For use in the in vitro quantitative Recalled...
The Issue: Potential for the VITROS 5600 Integrated System to dispense an insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DX-D 600 Product Usage: The DX-D 600 system is a Recalled by Agfa N.V. Due...
The Issue: A supplier for the Agfa system noted a potential for the steel support...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Permobil powered wheelchairs Recalled by Permobil, Ab Due to This correction...
The Issue: This correction decision has been made because of a potential failure of one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. Recalled by...
The Issue: Monopolar Curved Scissor (MCS) instruments may be susceptible to developing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X/Xi EndoWrist 8mm Monopolar Curved Scissors Model No. Recalled by...
The Issue: Monopolar Curved Scissor (MCS) instruments may be susceptible to developing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Megestrol Acetate Oral Suspension Recalled by Mckesson Corporation Due to...
The Issue: Supterpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Institutional,...
The Issue: Failed Impurities/Degradation Specifications; out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.