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-Prolo, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0558, NDC 73069-443-41. 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-Collagen, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0085, NDC 73069-095-41. 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-Infla, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0279, NDC 73069-249-41. 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 3, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0463, NDC 73069-373-41. 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-Articula, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0031, NDC 73069-037-41. 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-Systemic Detox, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0665, NDC 73069-500-41. 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-Adipose, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0008, NDC 73069-024-41. 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-Ithurts, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0290, NDC 73069-270-41. 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-Ouch, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0500, NDC 73069-402-41. 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-MuSkel-Neural, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC4020, NDC 73069-347-41. 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-Connectissue, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0090, NDC 73069-100-41. 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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