Drug recall
Ascorbic Acid Sterile Injection Solution, 500 mg/mL, 50 mL vial, Non-Corn Source, Rx only, Atlas…
FDA recall event 83710 · Class II · Atlas Pharmaceuticals, LLC
Key facts
| Event ID | 83710 |
|---|---|
| Recall numbers | D-0144-2020 |
| Recalling firm | Atlas Pharmaceuticals, LLC |
| Product type | Drugs |
| Products | 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. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Labeling: Not Elsewhere Classified; product is labeled as "Non-Corn Source" however the product is from a corn source. |
| Initiation date | Aug 28, 2019 |
| Report date | Oct 23, 2019 |
| Termination date | Jun 3, 2020 |
| City | Phoenix |
| State | AZ |
| Country | United States |
| FEI number | 3013030904 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: