8046255 Canada Inc. DBA Viatrexx Recalls 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
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
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
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
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
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
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
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
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
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
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
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
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 →
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.
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