FDAFDA · Food and drugs·Recall number D-0144-2020
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.
Published October 23, 2019 · Recall initiated: August 28, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling: Not Elsewhere Classified; product is labeled as "Non-Corn Source" however the product is from a corn source.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Atlas Pharmaceuticals, LLC
- Distributor
- Healthcare facilities/clinics in AZ and CO
- Lot
- Lot #: S-60162, BUD 10/12/2019; S-60176, BUD 11/2/2019; S-60187, BUD 11/11/2019; S-60189, BUD 11/16/2019; S-60190, BUD 11/16/2019; S-60222, BUD 01/20/2020
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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