FarmaKeio Testosterone Pellets: Metal Particulate Risk in Drug Product

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Contact the company & request your remedy

Recalling firmFARMAKEIO OUTSOURCING LLC920 S Kimball Ave Ste 100, N/A · Southlake, TX 76092-9019

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✎ GovInfoNow plain-language explainer

What happened, in plain English

FarmaKeio is recalling testosterone pellets that may contain metal particles. This could cause injury if the particles enter the body during injection. The product is prescription-only and sold under specific lot numbers.

Why it’s dangerous

The product was manufactured under CGMP deviations that could lead to metal particles being present. If these particles enter the body during subcutaneous injection, they could cause injury or infection.

Who’s affected

Prescription patients using these testosterone pellets for hormone replacement therapy. Those with the specific lot numbers listed in the recall are most at risk.

How to tell if you have this one

Check your prescription label for the lot numbers: 3090 (exp 1/7/2026), 3181 (exp 2/11/2026), or 3189/3190 (exp 2/12/2026). The product is a sterile pellet for subcutaneous injection only.

Brand
FarmaKeio
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Your Product
Look for the lot numbers on your prescription label: 3090 (exp 1/7/2026), 3181 (exp 2/11/2026), or 3189/3190 (exp 2/12/2026).

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The product has been recalled due to potential metal particles. Do not use it until you confirm it's not recalled.

What should I do if I have this product?

Check your prescription label for the lot numbers listed. If you have the recalled lot numbers, contact your doctor or the manufacturer.

How can I get a replacement?

The recall record does not specify a replacement process. Contact your doctor or the manufacturer for guidance.

Take action

Contact FarmaKeio

We’ve drafted a message you can send FarmaKeio to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-0134-2026 — FarmaKeio FarmaKeio

Hello,

I own a FarmaKeio that is covered by recall D-0134-2026 from FarmaKeio.

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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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-0134-2026 (October 14, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0134-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.

FARMAKEIO OUTSOURCING LLC recalls Testosterone / Triamcinolone Acetonide, 62.5MG/12.5MCG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY,

Recall notice