Sermorelin Forte Plus 27 mg recalled over sterility concerns
- Recall date
- November 17, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Tri-Coast Pharmacy recalls Sermorelin Forte Plus 27 mg (Sermorelin Acetate 9 mg/GHRP-6 9 mg/GHRP-2 9 mg). Compounded by Tri-Coast Pharmacy
- Recall number
- D-0293-2017
- FDA classification
- Class II
- Brand / firm
- Tri-Coast Pharmacy
- Sold / distributed
- Nationwide
Why it was recalled
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
Sermorelin Forte Plus 27 mg (Sermorelin Acetate 9 mg/GHRP-6 9 mg/GHRP-2 9 mg). Compounded by Tri-Coast Pharmacy
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