Ascorbic Acid 500 mg/ml Injectable Vial recalled over sterility concerns
- Recall date
- June 2, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- The Compounding Pharmacy of America recalls Ascorbic Acid 500 mg/ml Injectable Vial, Sterile Multi-Dose Vial, Refrigerate, The Compounding Pharmacy of America, Kno…
- Recall number
- D-1442-2015
- FDA classification
- Class II
- Brand / firm
- The Compounding Pharmacy of America
- Sold / distributed
- Nationwide
Why it was recalled
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Ascorbic Acid 500 mg/ml Injectable Vial, Sterile Multi-Dose Vial, Refrigerate, The Compounding Pharmacy of America, Knoxville, TN
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