Ascorbic Acid Sterile Injection Solution — Class II drug recall D-0144-2020
Terminated recall by Atlas Pharmaceuticals, LLC, reported 2019-10-23, distributed in AZ, CO. Labeling: Not Elsewhere Classified; product is labeled as "Non-Corn Source" however the product is from a corn
| Recall number | D-0144-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Atlas Pharmaceuticals, LLC, Phoenix, AZ, United States |
| Recall initiated | 2019-08-28 |
| Classified | 2019-10-15 |
| Reported by FDA | 2019-10-23 |
| Terminated | 2020-06-03 |
| Distributed | AZ, CO |
| Quantity | 1,646 vials |
| Reason classes | labeling |
| NDC | 71591-0500-50 |
| Lot numbers | S-60162, S-60176, S-60187, S-60189, S-60190, S-60222 |
| Expiration dates | 2019-10-12, 2019-11-02, 2019-11-11, 2019-11-16, 2020-01-20 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0144-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.