Glutathione 200mg/mL inj recalled over sterility concerns
- Recall date
- April 8, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Customceutical Compounding recalls Glutathione 200mg/mL inj. a) 10 ML and b) 12 ML MULTIDOSE VIAL MDV Compounded. Customceutical Compounding 4611 E. Shea…
- Recall number
- D-1255-2019
- FDA classification
- Class II
- Brand / firm
- Customceutical Compounding
- Sold / distributed
- U.S.A. Nationwide
Why it was recalled
Lack of assurance of sterility for injectables and solutions intended to be sterile.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Glutathione 200mg/mL inj. a) 10 ML and b) 12 ML MULTIDOSE VIAL MDV Compounded. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272
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