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Class II: temporary or reversible health riskOngoing

Farmakeio Outsourcing Testosterone / Triamcinolone Acetonide Pellet Recall

Testosterone / Triamcinolone Acetonide Pellet (200MG/40MCG), 1 PELLET (STERILE) FOR SUB…

FARMAKEIO OUTSOURCING LLC · Southlake, TX

Risk level
Class II
Reported by FDA
Nov 5, 2025
Recall ID
D-0137-2026
Check your lot numberHow we source this data

Summary

Farmakeio Outsourcing recalled Testosterone / Triamcinolone Acetonide Pellet starting Oct 14, 2025. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0137-2026 on Nov 5, 2025. Reason: CGMP Deviations: Potential presence of metal particulate matter. Status: Ongoing.

Why it was recalled

CGMP Deviations: Potential presence of metal particulate matter

Product description

Testosterone / Triamcinolone Acetonide Pellet (200MG/40MCG), 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0364-01

Lot numbers, UPCs & expiration codes

Lot, expiry: 3075, Exp 1/2/2026; 3084, Exp 1/6/2026; 3110, Exp 1/15/2026; 3115, Exp 1/16/2026; 3116, Exp 1/20/2026; 3119, Exp 1/21/2026; 3121, Exp 1/22/2026; 3124, Exp 1/23/2026; 3125, Exp 1/28/2026; 3131, Exp 1/29/2026; 3134, Exp 2/3/2026; 3135, Exp 2/4/2026; 3139, Exp 2/6/2026; 3204, Exp 2/13/2026; 3205, Exp 2/18/2026; 3207, Exp 2/19/2026; 3208, Exp 2/24/2026; 3211, Exp 2/25/2026; 3213, Exp 2/26/2026; 3216, Exp 2/27/2026; 3223, Exp 3/4/2026; 3225, Exp 3/5/2026; 3228, Exp 3/6/2026; 3248, Exp 3/19/2026; 3254, Exp 3/25/2026; 3258, Exp 3/31/2026; 3269, Exp 4/1/2026; 3270, Exp 4/10/2026.

Where it was sold

Nationwide in the USA and Antigua

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0137-2026
Classification
Class II
Status
Ongoing
Recall initiated
Oct 14, 2025
FDA report date
Nov 5, 2025
Quantity
264,664 pellets
Recall type
Voluntary: Firm initiated
Recalling firm
FARMAKEIO OUTSOURCING LLC

Original FDA data

Every field from FDA enforcement report D-0137-2026, exactly as published.

Show all FDA fields
City
Southlake
State
TX
Status
Ongoing
Country
United States
Event ID
97799
Address
920 S Kimball Ave Ste 100
Code information
Lot, expiry: 3075, Exp 1/2/2026; 3084, Exp 1/6/2026; 3110, Exp 1/15/2026; 3115, Exp 1/16/2026; 3116, Exp 1/20/2026; 3119, Exp 1/21/2026; 3121, Exp 1/22/2026; 3124, Exp 1/23/2026; 3125, Exp 1/28/2026; 3131, Exp 1/29/2026; 3134, Exp 2/3/2026; 3135, Exp 2/4/2026; 3139, Exp 2/6/2026; 3204, Exp 2/13/2026; 3205, Exp 2/18/2026; 3207, Exp 2/19/2026; 3208, Exp 2/24/2026; 3211, Exp 2/25/2026; 3213, Exp 2/26/2026; 3216, Exp 2/27/2026; 3223, Exp 3/4/2026; 3225, Exp 3/5/2026; 3228, Exp 3/6/2026; 3248, Exp 3/19/2026; 3254, Exp 3/25/2026; 3258, Exp 3/31/2026; 3269, Exp 4/1/2026; 3270, Exp 4/10/2026.
Postal code
76092-9019
Report date
Nov 5, 2025
Product type
Drugs
Recall number
D-0137-2026
Classification
Class II
Recalling firm
FARMAKEIO OUTSOURCING LLC
Product quantity
264,664 pellets
Reason for recall
CGMP Deviations: Potential presence of metal particulate matter
Voluntary / mandated
Voluntary: Firm initiated
Product description
Testosterone / Triamcinolone Acetonide Pellet (200MG/40MCG), 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0364-01
Distribution pattern
Nationwide in the USA and Antigua
Recall initiation date
Oct 14, 2025
Initial firm notification
E-Mail
Center classification date
Oct 29, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0137-2026, published Nov 5, 2025. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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