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. 1,876 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,876 in last 12 months

Showing 1634116360 of 47,938 recalls

DrugJanuary 1, 2021· Precision Dose Inc.

Recalled Item: Chlorhexidine Gluconate Oral Rinse USP 0.12% Recalled by Precision Dose Inc....

The Issue: cGMP deviations: The firm was notified of the manufacturer's expanded recall.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2020· AuroMedics Pharma LLC

Recalled Item: Acetaminophen Injection 1 Recalled by AuroMedics Pharma LLC Due to...

The Issue: Discoloration and failed pH specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2020· Allergan, PLC.

Recalled Item: Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz Recalled by...

The Issue: Labeling: Missing instructions for use insert

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 30, 2020· Ocean Providence Minneapolis LLC

Recalled Item: Frozen Ground Tuna Recalled by Ocean Providence Minneapolis LLC Due to...

The Issue: Ground Tuna may contain elevated levels of Histamine.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 30, 2020· Beckman Coulter Inc.

Recalled Item: ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG - Product Recalled by Beckman...

The Issue: The Quality Control (QC) card has a label error for the standard deviation...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 28, 2020· Sunstar Americas, Inc.

Recalled Item: Paroex (Chlorhexidine Gluconate) Oral Rinse Recalled by Sunstar Americas,...

The Issue: cGMP Deviations; FDA inspection of manufacturing facility observed potential...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 28, 2020· Akorn, Inc.

Recalled Item: Levetiracetam Oral Solution Recalled by Akorn, Inc. Due to Defective...

The Issue: Defective container: Customer complaints for oral solution leaking from bottles.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 28, 2020· Mar-Med Co

Recalled Item: Tourni-Cot - Universal Recalled by Mar-Med Co Due to A failure can occur if...

The Issue: A failure can occur if the user attempts to remove the device by partially...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2020· Baxter Healthcare Corporation

Recalled Item: FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm...

The Issue: Potential for the battery to lose its ability to be recharged.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2020· Philips North America

Recalled Item: PHILIPS Incisive Computed tomography X-ray system Incisive CT Software...

The Issue: Patient tabletop moved out to the home position during scan initialization,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2020· Philips Ultrasound Inc

Recalled Item: Philips EPIQ Diagnostic Ultrasound System Recalled by Philips Ultrasound Inc...

The Issue: Control panel arm assembly could have missing or loose screws where undue...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 23, 2020· Shane Erickson Inc

Recalled Item: IMC Wash-Free Hand Sanitizer Recalled by Shane Erickson Inc Due to CGMP...

The Issue: CGMP Deviations: product manufactured at the same facility that produced...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2020· Shane Erickson Inc

Recalled Item: IMC Wash-Free Hand Sanitizer Recalled by Shane Erickson Inc Due to CGMP...

The Issue: CGMP Deviations: product manufactured at the same facility that produced...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2020· Shane Erickson Inc

Recalled Item: IMC Wash-Free Hand Sanitizer Recalled by Shane Erickson Inc Due to CGMP...

The Issue: CGMP Deviations: product manufactured at the same facility that produced...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2020· Fresenius Kabi USA, LLC

Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2020· Genus Lifesciences Inc.

Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by Genus Lifesciences Inc....

The Issue: Presence of Foreign Substance: Particulate matter was found in multiple lots...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 23, 2020· Combat Medical Systems, LLC

Recalled Item: Fresh Whole Blood Donor Set (P/N 80-801-D NSN 6515016640306) . Recalled by...

The Issue: There is the potential of a bent or disconnected needle in one of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 23, 2020· Combat Medical Systems, LLC

Recalled Item: Valkyrie LTOWB Collection (P/N 80-820 Recalled by Combat Medical Systems,...

The Issue: There is the potential of a bent or disconnected needle in one of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 23, 2020· Combat Medical Systems, LLC

Recalled Item: Fresh Whole Blood Transfusion Set (P/N 80-801 NSN 6515016574750) . Recalled...

The Issue: There is the potential of a bent or disconnected needle in one of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 23, 2020· Combat Medical Systems, LLC

Recalled Item: Valkyrie LTOWB Administration (P/N 80-821 NSN 6515016862401). Blood...

The Issue: There is the potential of a bent or disconnected needle in one of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing