Tailor Made Compounding recalls Tesamorelin, 1mg/vial, 6mL vial, Lyophilized Powder for Reconstitution and Subcutaneous Injection, Rx Only, Tailor Made
Tailor Made Compounding recalls specific lots of Tesamorelin vials with incorrect expiration dates. The vials list a 1-year expiration instead of the required 6 months. Consumers should check their vial lot numbers and contact the manufacturer for details.
Lower-risk recall
Labeling: Incorrect or Missing Lot and/or Expiration Date; vial indicates a 1 year expiration date instead of a 6 month expiration date
Contact the company & request your remedy
What happened, in plain English
Tailor Made Compounding is recalling specific lots of Tesamorelin vials that incorrectly list a 1-year expiration date instead of the required 6 months. This could lead to improper medication storage or use if the vial is used after its actual expiration date. Read more at govinfonow.com/recall/39546-tailor-made-compounding-tesamorelin-vials-have-incorrect-expiration-dates.
Source Summary by GovInfoNow · govinfonow.com/recall/39546-tailor-made-compounding-tesamorelin-vials-have-incorrect-expiration-dates · Updated October 6, 2026 · FDA enforcement record: FDA #D-0223-2019
Cite this page
“Tailor Made Compounding Tesamorelin Vials Have Incorrect Expiration Dates.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39546-tailor-made-compounding-tesamorelin-vials-have-incorrect-expiration-dates. Based on FDA recall #D-0223-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0223-2019%22&limit=1).
Why it’s dangerous
The vials incorrectly state a 1-year expiration date instead of the 6-month expiration date. This could mean the medication may degrade or become ineffective if used after the actual expiration date, potentially leading to improper treatment.
Who’s affected
People who have received the recalled Tesamorelin vials from Tailor Made Compounding for medical use. Those with the specific lot numbers listed in the recall are most at risk.
How to tell if you have this one
Check the lot number on the vial. The recalled lots include specific numbers like 7101804, 7111807, and others listed in the recall notice. The vials are labeled as Tesamorelin, 1mg/vial, 6mL vial, Lyophilized Powder for Reconstitution and Subcutaneous Injection.
- Brand
Tailor Made Compounding- Category
Drug
What to do — step by step
Check Vial Lot Number
Look for the lot number on the vial, which should match one of the listed numbers in the recall (e.g., 7101804, 7111807).
Questions people ask
Why is this vial being recalled?
The vials incorrectly list a 1-year expiration date instead of the required 6-month expiration date, which could lead to medication degradation or ineffectiveness.
How do I know if my vial is part of this recall?
Check the lot number on the vial against the list provided in the recall notice, which includes specific numbers like 7101804, 7111807, and others.
What should I do if I have a recalled vial?
Contact Tailor Made Compounding directly to confirm your vial's status and follow their instructions.
Contact Tailor Made Compounding
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-0223-2019 — Tailor Made Compounding Tailor Made Compounding Hello, I own a Tailor Made Compounding that is covered by recall D-0223-2019 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.
Similar recalls
Keep exploring
From people who’ve dealt with this
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
Where this comes from
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.
- Official source: FDA Recall #D-0223-2019 (September 28, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0223-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
