Sermorelin/GHRP-6 Injection 6 mg-3 mg Lyophylized I recalled over sterility concerns
- Recall date
- August 1, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Town and Country Compounding and Consultation Services recalls Sermorelin/GHRP-6 Injection 6 mg-3 mg Lyophylized I, 2 mL vial, Rx, Town and Country Compounding and Consultation Servi…
- Recall number
- D-0228-2017
- FDA classification
- Class I
- Brand / firm
- Town and Country Compounding and Consultation Services
- Sold / distributed
- MA, NY, NJ & FL; Canada
Why it was recalled
Non-Sterility; microbial contamination identified as Bacillus circulans
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
What was recalled
Sermorelin/GHRP-6 Injection 6 mg-3 mg Lyophylized I, 2 mL vial, Rx, Town and Country Compounding and Consultation Services, Ridgewood, NJ 074502
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