FDAFDA · Food and drugs·Recall number D-0343-2020
Viatrexx-Intra-Cell, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0280, NDC 73069-250-41.
Published November 20, 2019 · Recall initiated: October 15, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- 8046255 Canada Inc. DBA Viatrexx
- Distributor
- Distributed to physicians Nationwide throughout the United States and Puerto Rico.
- Lot
- Lot Numbers: 19-S00025, Exp. May: 2020
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- Canada
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