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. 1,091 recalls have been distributed to North Dakota in the last 12 months.
Showing 601–620 of 27,512 recalls
Recalled Item: Parasite Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neurotransmitters Plus Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adrenal Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Female Fertility Test Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leaky Gut Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allergy test Small Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liver Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Urinary Tract Infection Test Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Candida Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HPV Antigen Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iron Deficiency Test Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pregnancy Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBS Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution without...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Downstream Occlusion alarms may occur during procedures using low flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaginal PH Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP50. Product Number: M8004A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP2. Product Number: M8102A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Multi-Measurement Module X3. Product Number: 867030. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX600. Product Number: 865242. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX500. Product Number: 866064. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.