Class II · ModerateActive recall
Testosterone / Triamcinolone Acetonide
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot: 3090, Exp 1/7/2026; 3181, Exp 2/11/2026; 3189, 3190, Exp 2/12/2026
Where it was soldNationwide in the USA and Antigua
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
CGMP Deviations: Potential presence of metal particulate matter
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | FARMAKEIO OUTSOURCING LLC |
| NDC | 73693-0366-01 |
Show the full FDA record
| Full product label | Testosterone / Triamcinolone Acetonide, 62.5MG/12.5MCG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0366-01 |
| Recalling firm | FARMAKEIO OUTSOURCING LLC |
| Distribution | Nationwide in the USA and Antigua |
| Quantity | 31,124 pellets |
| Recall initiated | 2025-10-14 |
| Report date | 2025-11-05 |
| Recall completed | — |
| Recall number | D-0134-2026 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | Southlake TX United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.