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. 1,032 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,032 in last 12 months

Showing 16001–16020 of 47,938 recalls

Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System...

The Issue: Due to not having the full complement of biological assessments for all...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Medtronic Vascular, Inc.

Recalled Item: Valiant Navion Thoracic Stent Graft System. For endovascular repair of...

The Issue: Due to the presence of type IIIb endoleaks, stent fractures, and stent ring...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: NUVASIVE FREEDOM: End Cap for PRECICE Intramedullary Limb Lengthening System...

The Issue: Due to not having the full complement of biological assessments for all...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: NUVASIVE PRECICE UNYTE System (Humerus and Tibia): PRECICE Trauma Nail...

The Issue: Due to not having the full complement of biological assessments for all...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: Precice Bone Transport - Product Usage: intended for limb lengthening...

The Issue: Due to complaints of adverse events potentially related to biological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS SARS-CoV-2 Antigen Reagent Pack - The VITROS Immunodiagnostic...

The Issue: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen False Reactive Results...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent- In Vitro...

The Issue: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen False Reactive Results...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: PRECICE STRYDE - Product Usage: intended for limb lengthening Recalled by...

The Issue: Due to complaints of adverse events potentially related to biological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2021· Hollister Incorporated

Recalled Item: Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and...

The Issue: The tube holder can separate from the barrier that secures the device to the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Epoprostenol Sodium for Injection Recalled by Teva Pharmaceuticals USA Due...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Metoclopramide Injection USP Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Sterile Diluent for Epoprostenol Sodium for Injection Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Desmopressin Acetate Injection USP Recalled by Teva Pharmaceuticals USA Due...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Dacarbazine for Injection USP Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Vecuronium Bromide for Injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund