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. 949 recalls have been distributed to North Dakota in the last 12 months.
Showing 35961–35980 of 47,938 recalls
Recalled Item: Safeway Care Loratadine Orally Disintegrating Tablets Recalled by Ohm...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TopCare LORATIDINE ORALLY DISINTEGRATING TABLETS Recalled by Ohm...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Health Mart Pharmacy loratadine orally disintegrating tablets Recalled by...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for z-statistic related to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...
The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xpert CT /NG Vaginal/Endocervical/ Specimen Collection Kit: Part number...
The Issue: Firm determined that some lots of CT/NG Swab 50 and CT/NG Urine collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xpert CT/NG Urine Specimen Collection Kit Part number GXCT/NGURINE-50...
The Issue: Firm determined that some lots of CT/NG Swab 50 and CT/NG Urine collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...
The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quickie IRIS Wheelchair. model EIZ4-2 in combination with option code...
The Issue: Quickie IRIS and Zippie IRIS tilt-in-space wheelchairs with MONO Backrest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...
The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ Folate Ascorbic Acid/Ascorbic Acid Diluent Recalled by...
The Issue: Low red blood cell control recoveries and low results for red blood cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...
The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.