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. 2,557 recalls have been distributed to North Dakota in the last 12 months.
Showing 3641–3660 of 47,938 recalls
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) CENTRAL LINE DRESSING KIT Recalled by...
The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) Port Access Kit Recalled by MEDLINE...
The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) SHORT TERM INFUSAPORT ACCESS KIT...
The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 820 ISO Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 850 SEV Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnVisio Patient Pad Transition Cushion Recalled by Elucent Medical Inc Due...
The Issue: There is a potential safety risk caused by physical disassociation of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 6 Plus Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 850 ISO Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 820 SEV Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT and Spectral CT Plus. Model Numbers: 728333 Recalled by Philips...
The Issue: Potential for a plan box not updated issue during Interventional procedure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.