Tailor Made Compounding recalls specific batches of Melanotan I 200mcg/mL vials due to lack of sterility assurance. Affected vials may cause infections if used.
Lack of Assurance of Sterility
Tailor Made Compounding is recalling certain batches of Melanotan I 200mcg/mL vials because they lack sterility assurance. Using these vials could lead to infections if injected.
The vials were manufactured without proper sterility checks, meaning they could contain harmful bacteria. If injected, this could cause infections or other health issues.
People who purchased or use Tailor Made Compounding's Melanotan I 200mcg/mL vials (1.5mL or 5mL) from the listed batches. Those with medical conditions requiring injections are at higher risk.
Check for batch numbers: 01072212A1 (exp 4/7/2022), 03032220A1 (exp 6/1/2022), 12162120A2 (exp 3/16/2022), 01142205A1 (exp 4/14/2022), 02012226A1 (exp 5/2/2022), or 03032220A1 (exp 6/1/2022). The vials are labeled as 1.5mL or 5mL and require refrigeration.
Look for batch numbers on the vial: 01072212A1, 03032220A1, 12162120A2, 01142205A1, 02012226A1, or 03032220A1.
Tailor Made Compounding is recalling specific batches of Melanotan I 200mcg/mL vials (1.5mL and 5mL) due to lack of sterility assurance.
Check the batch number on the vial: 01072212A1 (exp 4/7/2022), 03032220A1 (exp 6/1/2022), 12162120A2 (exp 3/16/2022), 01142205A1 (exp 4/14/2022), 02012226A1 (exp 5/2/2022), or 03032220A1 (exp 6/1/2022).
The recall does not specify a disposal action, so you should check with the manufacturer if you have the recalled batch numbers.
We’ve drafted a message you can send Tailor Made Compounding to request your refund or repair — edit it as you like.
Subject: Recall D-1212-2022 — Tailor Made Compounding Tailor Made Compounding Hello, I own a Tailor Made Compounding that is covered by recall D-1212-2022 from Tailor Made Compounding. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
