Class II · Moderate risk
Melanotan II 1 mg/mL
Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Is Melanotan recalled?
Yes — there is an active recall. 1 ongoing FDA recall mention Melanotan (3 total). Check the affected lots below.
Most common reason: Sterility / contamination (3 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Melanotan. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Melanotan recalls on record
none so far in 2026; 3 on record, newest first
Class II · Moderate risk
Melanotan I 200mcg/mL
Lack of Assurance of Sterility
Class II · Moderate risk
Melanotan II
Lack of sterility assurance.
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