Drug & medication recalls Moderate risk

BPC-157/Thymosin Beta-4 for Injection recalled over sterility concerns

Recall date
July 30, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
GenoGenix LLC recalls BPC-157/Thymosin Beta-4 for Injection, a) 10/10mg, b) 15/15mg, c) 15mg/15mg, all presentations, GenoGenix, LLC, 2840 NW…
Recall number
D-0086-2026
FDA classification
Class II
Brand / firm
GenoGenix LLC
Sold / distributed
US 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

BPC-157/Thymosin Beta-4 for Injection, a) 10/10mg, b) 15/15mg, c) 15mg/15mg, all presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for CELIA Health, Extension Health and Medical Health Institute (MHI).

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