# FDA recall D-0144-2020

> **Atlas Pharmaceuticals, LLC** · Class II · drug recall initiated 2019-08-28.

## Product

Ascorbic Acid Sterile Injection Solution, 500 mg/mL, 50 mL vial, Non-Corn Source, Rx only, Atlas Pharmaceuticals, LLC, 711 E Carefree Hwy, Suite 107, Phoenix, AZ  85085, NDC 71591-500-50.

## Reason for recall

Labeling: Not Elsewhere Classified; product is labeled as "Non-Corn Source" however the product is from a corn source.

## Distribution

Healthcare facilities/clinics in AZ and CO

## Key facts

- **Recall number:** D-0144-2020
- **Recalling firm:** Atlas Pharmaceuticals, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-08-28
- **Report date:** 2019-10-23
- **Termination date:** 2020-06-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Phoenix, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0144-2020

## Citation

> AI Analytics. FDA recall D-0144-2020. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0144-2020. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*