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. 1,061 recalls have been distributed to North Dakota in the last 12 months.
Showing 7141–7160 of 47,938 recalls
Recalled Item: EZDilate Fixed Wire Balloon 18-19-20. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 11-12-13. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HIGH PRESSURE ROTATOR WITH FEMALE LUER LOCK Recalled by Smiths Medical Asd...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1050 STOPCOCK LEFT ROTATOR OFF HANDLE Recalled by Smiths Medical Asd Inc Due...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HIGH PRESSURE ROTATOR WITH MALE LUER LOCK Recalled by Smiths Medical Asd Inc...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 18-19-20. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 8.5-9.5-10.5. indicated for endoscopic dilation...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medex 700PSI STOPCOCK W/ROTATOR Recalled by Smiths Medical Asd Inc Due to...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medex 20IN (50.8CM) INJ LINE ROTATING ADAPT Recalled by Smiths Medical Asd...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 48IN (121.9CM) INJ LINE ROTATING ADAPT (900psi) Recalled by Smiths Medical...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: neostigmine methylsulfate 5 mg/5 mL Injection Recalled by SCA...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride Recalled by SCA...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Citrate 4% 3 mL Recalled by SCA Pharmaceuticals, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 500 mcg/100 mL Recalled by SCA Pharmaceuticals, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl 800 mcg/10 mL in 0.9% Sodium Chloride Injection Recalled...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl 400 mcg/10 mL in 0.9% Sodium Chloride Injection Recalled...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SUCcinylcholine Chloride 100 mg/5mL Injection (Concentration = 20mg/mL)...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone HCl 20 mg/100mL in 0.9% Sodium Chloride Injection Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl 800 mcg/10 mL in 0.9% Sodium Chloride Injection Recalled...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone HCl 25 mg/25 mL in 0.9% Sodium Chloride Injection Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.