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Class IIOngoing

Tesamorelin for Injection recall

FDA recall D-0088-2026 · initiated Jul 30, 2025

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Oct 15, 2025How we research

GenoGenix LLC recalled Tesamorelin for Injection in Jul 2025 — an FDA Class II recall (D-0088-2026) because Lack of Assurance of Sterility.

May cause temporary or medically reversible harm; low probability of serious harm.

Why it was recalled

Lack of Assurance of Sterility

Sterility could not be assured

The maker could not guarantee the product was sterile. That matters most for injections and eye products, where a contaminated dose reaches past the body's defences.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

Lot#: GG020425-004 within expiry.

Details

Product
Tesamorelin for Injection, 15mg, 10 mL Multi-Dose Vial, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Recalling company
GenoGenix LLC
Classification
Class II
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
US Nationwide.
Initiated
Jul 30, 2025
FDA report date
Oct 15, 2025
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was Tesamorelin for Injection recalled?
GenoGenix LLC recalled Tesamorelin for Injection in Jul 2025 — an FDA Class II recall (D-0088-2026) because Lack of Assurance of Sterility. May cause temporary or medically reversible harm; low probability of serious harm.
Why was Tesamorelin for Injection recalled?
Per the FDA enforcement record, the reason for recall D-0088-2026 was: Lack of Assurance of Sterility
Is a recalled Tesamorelin for Injection dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of Tesamorelin for Injection are affected?
Distributed: US Nationwide.. The recall covers these lots — Lot#: GG020425-004 within expiry.. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0088-2026.

Source: openFDA Drug Enforcement record D-0088-2026

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