People's Custom Rx C-PROGESTERONE OIL 100 MG/ML Vials Recall: Non-Sterility Hazard
People's Custom Rx recalls 10mL C-PROGESTERONE OIL vials (lot 11649, batch 07/07/2021) due to non-sterility risk. Consumers should contact the company for details.
Recall notice
Non-Sterility
Contact the company
What happened, in plain English
People's Custom Rx is recalling 10mL C-PROGESTERONE OIL vials that may not be sterile. This could lead to infections if used improperly. Affected users should stop using the product and contact the manufacturer. Read more at govinfonow.com/recall/36150-people-s-custom-rx-c-progesterone-oil-100-mg-ml.
Source Summary by GovInfoNow · govinfonow.com/recall/36150-people-s-custom-rx-c-progesterone-oil-100-mg-ml · Updated October 4, 2026 · FDA enforcement record: FDA #D-0718-2021
Cite this page
“People's Custom Rx C-PROGESTERONE OIL 100 MG/ML Vials Recall: Non-Sterility Hazard.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36150-people-s-custom-rx-c-progesterone-oil-100-mg-ml. Based on FDA recall #D-0718-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0718-2021%22&limit=1).
Why it’s dangerous
Non-sterility means the product may contain harmful bacteria or contaminants. This could cause infections if the medication is used without proper sterilization.
Who’s affected
People who have received this compounded hormone treatment from People's Custom Rx in Memphis, TN. Those using the product for medical purposes are most at risk.
How to tell if you have this one
Check for vials labeled 'C-PROGESTERONE OIL 100 MG/ML, 10 mL' from People's Custom Rx. The batch date is 07/07/2021 and lot number 11649.
- Brand
People's Custom Rx- Category
Drug
What to do — step by step
Contact Manufacturer
Reach out to People's Custom Rx at 785 E Brookhaven Cir, Memphis, TN 38117 for specific instructions on handling the recalled product.
Where it went and when
Where it was distributed
Distributed in Mississippi and Tennessee.
FDA distribution: “MS, TN” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Mississippi, Tennessee.
Recall timeline
FDA terminated this recall 3.3 years after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Is this product safe to use?
The recall indicates a non-sterility hazard, so the product may not be safe. Do not use until contacted by the manufacturer.
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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-0718-2021 (May 11, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0718-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 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.