Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

New Vitalis Pharmacy LLC dba New Vitalis Pharmacy: Testosterone Injection Solution Recalled for Lack of Sterility Assurance

Agency Publication Date: November 22, 2019
Share:
Sign in to monitor this recall

Summary

New Vitalis Pharmacy has recalled approximately 2,982 units of Testosterone Cypionate/Testosterone Propionate Oil Injection Solution because the pharmacy cannot guarantee the products are sterile. Using an injectable medication that is not sterile can lead to serious and potentially life-threatening infections. The affected products were distributed nationwide in 10 mL vials and include various lot numbers with expiration dates ranging from September 2019 through November 2019. If you have this medication, you should immediately contact your doctor or pharmacist to discuss your treatment options and how to safely return the product.

Risk

A lack of sterility assurance means the injectable drug may contain bacteria, fungi, or other contaminants. Injecting a non-sterile product directly into the body can cause localized infections at the injection site or systemic infections that can lead to severe illness or death.

What You Should Do

  1. Check your medication vials for Testosterone Cypionate 180 mg/mL/Testosterone Propionate 20mg/mL Oil Injection Solution (10 mL per vial) from New Vitalis Pharmacy.
  2. Identify if your vial matches one of the following lot numbers and expiration dates: AL-07232019@99 (Exp 9-23-2019), AL-07312019@99 (Exp 9-30-2019), AL-08132019@99 (Exp 10-13-2019), AL-08272019@901 (Exp 10-27-2019), AL-08282019@909 (Exp 10-28-2019), or Al-09032019@903 (Exp 11-3-2019).
  3. Immediately stop using any affected medication and consult your healthcare provider or pharmacist regarding the risks and to obtain a replacement.
  4. Return any unused product to the pharmacy where you purchased it for a refund and contact New Vitalis Pharmacy for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for more information.

Your Remedy Options

๐Ÿ’ฐFull Refund

Healthcare provider consultation and pharmacy refund.

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Testosterone Cypionate 180 mg/mL/Testosterone Propionate 20mg/mL Oil Injection Solution (10 mL vial)
Model:
D-0523-2020
Lot Numbers:
AL-07232019@99 (Exp 9-23-2019)
AL-07312019@99 (Exp 9-30-2019)
AL-08132019@99 (Exp 10-13-2019)
AL-08272019@901 (Exp 10-27-2019)
AL-08282019@909 (Exp 10-28-2019)
Al-09032019@903 (Exp 11-3-2019)
Date Ranges: 9-23-2019, 9-30-2019, 10-13-2019, 10-27-2019, 10-28-2019, 11-3-2019

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84189
Status: Resolved
Manufacturer: New Vitalis Pharmacy LLC dba New Vitalis Pharmacy
Sold By: New Vitalis Pharmacy
Manufactured In: United States
Units Affected: 2981.62 mL
Distributed To: Nationwide
Agency Last Updated: November 25, 2019

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.