Drug & medication recalls Moderate risk

Ipamorelin Acetate/Sermorelin Acetate /mL Injection recalled over sterility concerns

Recall date
April 5, 2022
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding recalls Ipamorelin Acetate/Sermorelin Acetate (1 mg/1 mg)/mL (10 mL) Injection, 10 mL vials, Rx Only, Farmakeio 1736…
Recall number
D-0777-2022
FDA classification
Class II
Brand / firm
North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding
Sold / distributed
Nationwide within United States

Why it was recalled

Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Ipamorelin Acetate/Sermorelin Acetate (1 mg/1 mg)/mL (10 mL) Injection, 10 mL vials, Rx Only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081

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