HIGH

Advanced Pharmaceutical Technology Recalls Testosterone Pellets Due to Contamination Risk

Advanced Pharmaceutical Technology recalled 22,843 cartons of TESTO-100 CIII testosterone pellets on October 3, 2025. The recall follows a risk of microbial contamination that could compromise product sterility. Consumers and healthcare providers should stop using the product immediately and seek guidance.

Quick Facts at a Glance

Recall Date
October 3, 2025
Hazard Level
HIGH
Brand
Advanced Pharmaceutical Technology
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
3 states
At-Risk Groups
GENERAL

Hazard Information

Lack of Assurance of Sterility: Potential microbial contamination of subcutaneous pellets.

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Advanced Pharmaceutical Technology, Inc. or your healthcare provider for guidance. Notification method: Letter

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

Product Details

The recall involves TESTO-100 CIII testosterone pellets, 100 mg, sold in cartons of 10 sterile pellets. The affected lot number is P-22-3, with an expiration date of June 2027. The product was distributed in Georgia, New York, Texas, Puerto Rico, the United Kingdom, Malta, and Greece.

The Hazard

The recall stems from a lack of assurance of sterility due to potential microbial contamination of the subcutaneous pellets. Contaminated products may pose serious health risks to users.

Reported Incidents

There have been no reported injuries or illnesses associated with this recall as of the latest report date. Zero incidents have been documented.

What to Do

Consumers should stop using the product immediately. Contact Advanced Pharmaceutical Technology or a healthcare provider for further instructions. A notification letter will be sent to affected parties.

Contact Information

For more information, consumers can visit https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0258-2026 or contact Advanced Pharmaceutical Technology directly.

Key Facts

  • Recall date: October 3, 2025
  • Quantity recalled: 22,843 pellets
  • Affected lot number: P-22-3
  • Expiration date: June 2027
  • Distribution states: GA, NY, TX, Puerto Rico, UK, Malta, Greece

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
Lot #: P-22-3
Exp 06-2027
Affected States
GA, NY, TX
Report Date
January 21, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

Related Recalls

HIGH

Fresenius Kabi Vancomycin Injection Recalled Over Sterility Concerns

Fresenius Kabi Compounding recalled its vancomycin HCl injection on February 5, 2026, due to a lack of assurance of sterility. This Class II recall affects all lots distributed nationwide. Healthcare providers and consumers must stop using the product immediately.

Fresenius Kabi Compounding
Lack of
Read more
HIGH

Fresenius Kabi Compounding Issues Recall of Vancomycin Injection

Fresenius Kabi Compounding recalled 1,578 bags of vancomycin HCl injection on February 5, 2026. The company cited a lack of assurance of sterility as the reason for the recall. Healthcare providers and consumers should stop using the product immediately.

Fresenius Kabi Compounding
Lack of
Read more
HIGH

Pro Numb Tattoo Numbing Spray Recalled Due to cGMP Violations

Pro Numb Tattoo Numbing Spray was recalled on February 2, 2026 due to cGMP deviations. The product, containing 4% lidocaine, is distributed by Pro Numb Tattoo Numbing Spray LLC. Consumers should stop using it immediately and contact the company for further guidance.

PRO NUMB SENSITIVE SKIN
cGMP deviations
Read more