TRIOVA PHARMACEUTICALS LLC recalls Estriol USP Micronized 5 G, Rx only, Triova 115 W 3rd Street Suite 720 Tulsa, OK 74103, NDC 71092-9977-02
Triova recalls Estriol USP Micronized 5g (NDC 71092-9977-02) due to failed impurities testing. This medication may contain harmful substances that could affect safety.
Recall notice
Failed impurities/ degradation specifications: Out of specification for organic impurities.
Contact the company & request your remedy
What happened, in plain English
Triova is recalling Estriol USP Micronized 5g (Rx only) because it failed impurities testing. This could mean the product contains harmful substances that might affect your health. Read more at govinfonow.com/recall/37116-triova-estriol-micronized-5g-recall-failed-impurities-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/37116-triova-estriol-micronized-5g-recall-failed-impurities-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1284-2020
Cite this page
“Triova Estriol Micronized 5g Recall: Failed Impurities Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37116-triova-estriol-micronized-5g-recall-failed-impurities-risk. Based on FDA recall #D-1284-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1284-2020%22&limit=1).
Why it’s dangerous
The product failed impurities testing, meaning it may contain harmful substances that could affect safety. This is a quality issue that could lead to health risks if the impurities are not properly controlled.
Who’s affected
People with prescriptions for this medication are affected. Those using it for hormone replacement therapy may be at higher risk.
How to tell if you have this one
Check for the product name 'Estriol USP Micronized 5g' with NDC 71092-9977-02. The lot number starts with 17010401181119190927 and expires by December 2020.
- Brand
Triova- Category
Drug
What to do — step by step
Check Product Details
Look for the NDC code 71092-9977-02 and lot number starting with 17010401181119190927 on the label.
Questions people ask
Is this product safe to use?
The official notice states the product failed impurities testing, so it may contain harmful substances. Do not use until the recall is resolved.
What should I do if I have this product?
The recall record does not specify a remedy, so contact your healthcare provider for guidance.
How can I check if my product is recalled?
Check the NDC code 71092-9977-02 and lot number starting with 17010401181119190927 on the label.
Contact Triova
We’ve drafted a message you can send Triova to request your refund or repair — edit it as you like.
Subject: Recall D-1284-2020 — Triova Triova Hello, I own a Triova that is covered by recall D-1284-2020 from Triova. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
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-1284-2020 (May 15, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1284-2020 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.