D-0343-2020 Class II Terminated

Recalled by 8046255 Canada Inc. DBA Viatrexx — Beloeil, N/A

Recall Details

Product Type
Drugs
Report Date
November 20, 2019
Initiation Date
October 15, 2019
Termination Date
December 10, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
8 vials

Product Description

Viatrexx-Intra-Cell, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0280, NDC 73069-250-41.

Reason for Recall

Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.

Distribution Pattern

Distributed to physicians Nationwide throughout the United States and Puerto Rico.

Code Information

Lot Numbers: 19-S00025, Exp. May: 2020