Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Testosterone Cypionate/Proprinate 200 mg/10 mg/1 mL 30 mL Injectable Recalled by Pharm D Solutions, LLC Due to Lack of Assurance of Sterility

Date: September 10, 2018
Company: Pharm D Solutions, LLC
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Pharm D Solutions, LLC directly.

Affected Products

Testosterone Cypionate/Proprinate 200 mg/10 mg/1 mL 30 mL Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1745-30

Quantity: 580 vials and 30000 milliliters

Why Was This Recalled?

Lack of Assurance of Sterility

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Pharm D Solutions, LLC

Pharm D Solutions, LLC has 100 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report