PlainRecalls
FDA Drug Moderate Class II Terminated

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.

Reported: October 23, 2019 Initiated: August 28, 2019 #D-0144-2020

Product Description

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.

Details

Units Affected
1646 vials
Distribution
Healthcare facilities/clinics in AZ and CO
Location
Phoenix, AZ

Frequently Asked Questions

What product was recalled?
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.. Recalled by Atlas Pharmaceuticals, LLC. Units affected: 1646 vials.
Why was this product recalled?
Labeling: Not Elsewhere Classified; product is labeled as "Non-Corn Source" however the product is from a corn source.
Which agency issued this recall?
This recall was issued by the FDA Drug on October 23, 2019. Severity: Moderate. Recall number: D-0144-2020.