Testosterone / Triamcinolone Acetonide Pellet (100MG/20MCG)
Recalled by FARMAKEIO OUTSOURCING LLC
Drug recall
FARMAKEIO OUTSOURCING LLC
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
FARMAKEIO OUTSOURCING LLC has recalled Testosterone / Triamcinolone Acetonide Pellet (100MG/20MCG), according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on November 5, 2025 and was initiated on October 14, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Testosterone / Triamcinolone Acetonide Pellet (100MG/20MCG), with approximately 103,444 pellets affected. The company behind the recall is FARMAKEIO OUTSOURCING LLC, based in Southlake, TX. The FDA describes the product as: “Testosterone / Triamcinolone Acetonide Pellet (100MG/20MCG), 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0367-01”
Why was Testosterone / Triamcinolone Acetonide Pellet (100MG/20MCG) recalled?
According to the FDA, the stated reason for the recall is: “CGMP Deviations: Potential presence of metal particulate matter.” In plain terms, this recall relates to foreign material.
A foreign material recall means that pieces of something which should not be in food — such as metal, plastic, or glass — may be present. These can pose a choking hazard or cause injury. Recalls like these are issued to remove the affected product before anyone is hurt.
What should you do?
If you think you may have bought Testosterone / Triamcinolone Acetonide Pellet (100MG/20MCG), compare it against the product description and identifying codes (Lot, expiry: 3098, 3101, Exp 1/8/2026; 3107, Exp 1/13/2026; 3108, Exp 1/14/2026; 3109, Exp 1/15/2026; 3230, Exp 3/10/2026; 3231, Exp 3/11/2026; 3235, Exp 3/13/…) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact FARMAKEIO OUTSOURCING LLC or your local health authority.
About this recall
This recall was distributed in TX. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Ongoing
- Date reported
- November 5, 2025
- Recall started
- October 14, 2025
- Distributed in
- TX
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Testosterone / Triamcinolone Acetonide Pellet (100MG/20MCG) recalled?+
According to the FDA: CGMP Deviations: Potential presence of metal particulate matter
How serious is this recall?+
Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
What should I do if I have Testosterone / Triamcinolone Acetonide Pellet (100MG/20MCG)?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: D-0136-2026. Information last synced from the FDA on July 6, 2026.