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.
Melanotan I 200mcg/mL
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Assurance of Sterility
Cause type: Sterility / contamination
A product that must be sterile could not be assured sterile, or was contaminated. A top reason for injectables, eye drops and IV products - loss of sterility assurance can lead to serious infections. All sterility / contamination recalls.
What was recalled
Melanotan I 200mcg/mL (2mg/ml), a) 1.5mL-vial, b) 5 mL-vial, Refrigerate, Tailor Made Compounding
Drug: Melanotan
- Recalling firm
- TMC Acquisition LLC dba Tailor Made Compounding
- Origin
- KY, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1212-2022 · FDA notice
Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall.
Other Melanotan recalls
See all
Class II · Moderate risk
Melanotan II
Lack of sterility assurance.
Other recalls by TMC Acquisition LLC dba Tailor Made Compounding
All 2022 recalls
Class II · Moderate risk
Glutathione 200mg/ml
Lack of Assurance of Sterility
Class II · Moderate risk
Vitamin D3 50
Lack of Assurance of Sterility
Class II · Moderate risk
Vitamin B-Complex Preservative Free
Lack of Assurance of Sterility
Class II · Moderate risk
Vitamin B-Complex
Lack of Assurance of Sterility
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