HYDROXO-B12 SDV 10MG/ML INJ recalled over sterility concerns
- Recall date
- April 18, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Key Pharmacy and Compounding Center recalls HYDROXO-B12 1ML SDV 10MG/ML INJ, Injection, 10mg/mL, Rx only, 1 mL glass/ Single Dose vial, Prepared by Key Compounding…
- Recall number
- D-0722-2017
- FDA classification
- Class II
- Brand / firm
- Key Pharmacy and Compounding Center
- Sold / distributed
- Distributed nationwide in U.S.A., Australia and Canada.
Why it was recalled
Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of 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
HYDROXO-B12 1ML SDV 10MG/ML INJ, Injection, 10mg/mL, Rx only, 1 mL glass/ Single Dose vial, Prepared by Key Compounding Pharmacy HYDROXO-B12 2ML SDV 10MG/ML INJ, Injection, 10mg/mL, RX only, 2 mL glass/ Single Dose vial.
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