# FDA recall D-0331-2020

> **8046255 Canada Inc. DBA Viatrexx** · Class II · drug recall initiated 2019-10-15.

## Product

Viatrexx-Systemic Detox, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0665, NDC 73069-500-41.

## Reason for recall

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

## Distribution

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

## Key facts

- **Recall number:** D-0331-2020
- **Recalling firm:** 8046255 Canada Inc. DBA Viatrexx
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-10-15
- **Report date:** 2019-11-20
- **Termination date:** 2020-12-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Beloeil, N/A, Canada

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0331-2020

## Citation

> AI Analytics. FDA recall D-0331-2020. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0331-2020. Source: US FDA. Licensed CC0.

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