8046255 Canada Inc. DBA Viatrexx
No ongoing recalls currently shown
Based on the official records currently available to Public Health Trace, no recalls naming 8046255 Canada Inc. DBA Viatrexx are currently shown as ongoing. The 23 records below are historical recall records.
Public Health Trace has 23 recalls naming 8046255 Canada Inc. DBA Viatrexx as the recalling firm, republished from official FDA and USDA sources.
Recall history - 23 terminated records Recalls by year
A bar chart of the number of recalls naming this company by year.
Recalls by year
Year Recalls 2019 23
Download CSV FDA Recall
Terminated Terminated: December 10, 2020 Historical record Class II
Viatrexx-ANS/CNS, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0025, NDC 73069-039-41. by 8046255 Canada Inc. DBA Viatrexx
Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility. Published
November 20, 2019 Distribution
Nationwide
View recall →
FDA Recall
Terminated Terminated: December 10, 2020 Historical record Class II
Viatrexx-Male+, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0400, NDC 73069-320-41. by 8046255 Canada Inc. DBA Viatrexx
Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility. Published
November 20, 2019 Distribution
Nationwide
View recall →
FDA Recall
Terminated Terminated: December 10, 2020 Historical record Class II
Viatrexx-Neuro, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0460, NDC 73069-375-41. by 8046255 Canada Inc. DBA Viatrexx
Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility. Published
November 20, 2019 Distribution
Nationwide
View recall →
FDA Recall
Terminated Terminated: December 10, 2020 Historical record Class II
Viatrexx-Hair, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0251, NDC 73069-206-41. by 8046255 Canada Inc. DBA Viatrexx
Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility. Published
November 20, 2019 Distribution
Nationwide
View recall →
FDA Recall
Terminated Terminated: December 10, 2020 Historical record Class II
Viatrexx-Facial, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0184, NDC 73069-164-41. by 8046255 Canada Inc. DBA Viatrexx
Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility. Published
November 20, 2019 Distribution
Nationwide
View recall →
FDA Recall
Terminated Terminated: December 10, 2020 Historical record Class II
Viatrexx-Intra-Cell, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0280, NDC 73069-250-41. by 8046255 Canada Inc. DBA Viatrexx
Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility. Published
November 20, 2019 Distribution
Nationwide
View recall →
FDA Recall
Terminated Terminated: December 10, 2020 Historical record Class II
Viatrexx-Relief +, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0615, NDC 73069-450-41. by 8046255 Canada Inc. DBA Viatrexx
Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility. Published
November 20, 2019 Distribution
Nationwide
View recall →
FDA Recall
Terminated Terminated: December 10, 2020 Historical record Class II
Viatrexx-Immunexx, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0270, NDC 73069-244-41. by 8046255 Canada Inc. DBA Viatrexx
Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility. Published
November 20, 2019 Distribution
Nationwide
View recall →
FDA Recall
Terminated Terminated: December 10, 2020 Historical record Class II
Viatrexx-Arthros, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0030, NDC 73069-035-41. by 8046255 Canada Inc. DBA Viatrexx
Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility. Published
November 20, 2019 Distribution
Nationwide
View recall →
FDA Recall
Terminated Terminated: December 10, 2020 Historical record Class II
Viatrexx-GI, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0211, NDC 73069-189-41. by 8046255 Canada Inc. DBA Viatrexx
Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility. Published
November 20, 2019 Distribution
Nationwide
View recall →
FDA Recall
Terminated Terminated: December 10, 2020 Historical record Class II
Viatrexx-Mesenchyme, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0092, NDC 73069-102-41. by 8046255 Canada Inc. DBA Viatrexx
Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility. Published
November 20, 2019 Distribution
Nationwide
View recall →
FDA Recall
Terminated Terminated: December 10, 2020 Historical record Class II
Viatrexx-Lymph 1, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0370, NDC 73069-310-41. by 8046255 Canada Inc. DBA Viatrexx
Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility. Published
November 20, 2019 Distribution
Nationwide
View recall →
Some FDA recall records on this page come from FDA's Enforcement Report database .
Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
This page lists recalls that name 8046255 Canada Inc. DBA Viatrexx as the recalling firm in the official source notice. It is
not a safety rating, ranking, or statement that the company acted negligently.
Read the full medical disclaimer .
