Stop using nowDrug recall · FDA · Published October 1, 2019
New Vitalis Pharmacy Recalls Testosterone Injections Due to Lack of Sterility
New Vitalis Pharmacy recalls testosterone injections with lot numbers AL-07232019 to AL-09032019 due to lack of sterility assurance. Consumers should not use these products.
“New Vitalis Pharmacy Recalls Testosterone Injections Due to Lack of Sterility.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37895-new-vitalis-pharmacy-recalls-testosterone-injections-due-to-lack-of. Based on FDA recall #D-0523-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0523-2020%22&limit=1).
The FDA announced on Oct. 1, 2019, that New Vitalis Pharmacy LLC is voluntarily recalling Testosterone Cypionate/Testosterone Propionate Oil Injection Solution due to a lack of sterility assurance. The recall affects product distributed nationwide in the USA.
How to tell if you have it
Brand: New Vitalis Pharmacy
Product: Testosterone Cypionate 180 mg/mL/Testosterone Propionate 20mg/mL Oil Injection Solution, 10 mL per vial
The product poses a hazard due to a lack of sterility assurance, according to the FDA.
Context
GovInfoNow's records show New Vitalis Pharmacy LLC has two other recalls on record since Sept. 22, 2021, including testosterone injections recalled on July 13, 2023, and testosterone vials recalled on Sept. 22, 2021, both due to lack of sterility assurance. Other recent recalls of similar products include New Life Pharma Semaglutide Injections Recall (Feb. 26, 2026), New Life Pharma Semaglutide Inj 2mg Vial Recall (Feb. 26, 2026), and New Life Pharma Tirzepatide Inj 15mg Vial Recall (Feb. 26, 2026).
How to tell if you have this one
Check the lot number on the vial, which starts with 'AL' followed by numbers and dates. The expiration dates range from September 23, 2019, to November 3, 2019.
Brand
New Vitalis Pharmacy
Category
Drug
Based on the official FDA remedy
What to do — step by step
Stop Using It Now
Immediately discard the recalled testosterone injections with lot numbers AL-07232019 to AL-09032019.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Distributed Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 3.4 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0523-2020 (October 1, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0523-2020 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 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.