Stop using now Drug recall · FDA · Published November 19, 2018

Pharm D Solutions Recalls HCG 3000 IU Due to Sterility Risk

Pharm D Solutions recalls Human Chorionic Gonadotropin 3000 IU vials due to lack of sterility assurance. Check lot 10292018:21.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0343-2019Drug Pharm D Solutions ›

Stop using this now

Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.

Take action

Contact the company

Recalling firmPharm D Solutions, LLC1304 S Loop W · Houston, TX 77054-4010

✎ GovInfoNow plain-language explainer

Pharm D Solutions, LLC is recalling Human Chorionic Gonadotropin 3000 IU because its manufacturing processes and equipment were inadequate to ensure the product remained sterile. This recall affects 85 vials distributed in Washington state that were sold with an expiration date of March 31, 2019. The specific lot number involved is 10292018:21. Read more at govinfonow.com/recall/39424-pharm-d-solutions-recalls-hcg-3000-iu-due-to-sterility.

Source Summary by GovInfoNow · govinfonow.com/recall/39424-pharm-d-solutions-recalls-hcg-3000-iu-due-to-sterility · Updated October 11, 2026 · FDA enforcement record: FDA #D-0343-2019

Cite this page

“Pharm D Solutions Recalls HCG 3000 IU Due to Sterility Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/39424-pharm-d-solutions-recalls-hcg-3000-iu-due-to-sterility. Based on FDA recall #D-0343-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0343-2019%22&limit=1).

The FDA announced on 2018-11-19 that Pharm D Solutions voluntarily recalled Human Chorionic Gonadotropin 3000 IU due to a lack of sterility assurance, according to the FDA. The recall affects 85 vials distributed in Washington state.

How to tell if you have it

Brand: Pharm D Solutions
Product: Human Chorionic Gonadotropin 3000 IU
NDC: 69699-1738-10
Lot: 10292018:21
Expiration Date: 3/31/2019

The hazard

The product poses a hazard due to inadequate processes and equipment to assure the sterility of products intended to be sterile, according to the FDA.

Context

GovInfoNow's records show Pharm D Solutions, LLC has 3 other recalls on record since 2016-10-12. Other recent recalls include Pharm D Solutions Recalls Ipamorelin Acetate Vials Due to Lack of Sterility Assurance (2019-05-23) and Pharm D Solutions, LLC recalls Slenderella Compound Injectable (2018-09-10). Similar recent recalls of sterile products include BD ChloraPrep Applicators Sterility Risk (2026-06-11), Apothecary Pharma Recalls Tirzepatide Injections Due to Sterility Risk (2026-09-24), and Reliance Bortezomib Injection Recall: Lack of Sterility Risk (2026-06-24).

How to tell if you have this one

Check if you have Human Chorionic Gonadotropin 3000 IU (Rx only) manufactured by Pharm D Solutions. Look for NDC 69699-1738-10 and Lot number 10292018:21 with an expiration date of 3/31/2019.

Brand
Pharm D Solutions
Category
Drug

Based on the official FDA remedy

What to do — step by step

Stop using the product
Do not use the recalled Human Chorionic Gonadotropin 3000 IU vials due to sterility concerns.
Contact the manufacturer
Call Pharm D Solutions at 1-844-263-6843 for further instructions regarding the recall.

Where it went and when

Where it was distributed

Distributed in Washington.

FDA distribution: “WA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Washington.

Recall timeline

FDA terminated this recall 23 months after the firm started it.

Nov 19, 2018Firm started the recall
Dec 20, 2018FDA classified it Class II
Dec 26, 2018Published in FDA’s Enforcement Report
Oct 13, 2020FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/39424-pharm-d-solutions-recalls-hcg-3000-iu-due-to-sterility">Pharm D Solutions Recalls HCG 3000 IU Due to Sterility Risk (GovInfoNow)</a>

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-0343-2019 (November 19, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0343-2019 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.