FDA recall record

GenoGenix BPC-157/Thymosin Beta-4 for Injection, a) 10/10mg, b) 15/15mg, c) 15mg/15mg, all recall — FDA D-0086-2026

Lack of Assurance of Sterility

Class IIclassification
D-0086-2026official record ID
Oct 15, 2025report date

Recall record at a glance

Official recordD-0086-2026
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmGenoGenix LLC
Report dateOct 15, 2025
Recall initiation dateJul 30, 2025
LocationBoca Raton, FL, United States

Official product description

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).

Why the product was recalled

Lack of Assurance of Sterility

Distribution information

US Nationwide.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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