Pharm D Solutions, LLC recalls Human Chorionic Gonadotropin 3000 IU, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054
Pharm D Solutions recalls Human Chorionic Gonadotropin 3000 IU (Rx only) because inadequate sterility processes may cause infections. NDC 69699-1738-10, Lot 10292018:21, Exp 3/31/2019.
Recall notice
Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.
Contact the company & request your remedy
What happened, in plain English
Pharm D Solutions is recalling Human Chorionic Gonadotropin 3000 IU (Rx only) because their manufacturing process may not ensure sterility. This could lead to infections if used improperly. Read more at govinfonow.com/recall/39424-pharm-d-solutions-recalls-human-chorionic-gonadotropin-3000-iu-due.
Source Summary by GovInfoNow · govinfonow.com/recall/39424-pharm-d-solutions-recalls-human-chorionic-gonadotropin-3000-iu-due · Updated October 5, 2026 · FDA enforcement record: FDA #D-0343-2019
Cite this page
“Pharm D Solutions recalls Human Chorionic Gonadotropin 3000 IU due to lack of sterility assurance.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39424-pharm-d-solutions-recalls-human-chorionic-gonadotropin-3000-iu-due. Based on FDA recall #D-0343-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0343-2019%22&limit=1).
Why it’s dangerous
The product may not be sterile due to inadequate manufacturing processes. If the product is not sterile, it could cause infections when injected, especially in medical settings where sterility is critical.
Who’s affected
People who have received this specific lot of Human Chorionic Gonadotropin 3000 IU for medical use. Those with compromised immune systems or open wounds are at higher risk.
How to tell if you have this one
Check the NDC number 69699-1738-10 and lot number 10292018:21 on the product label. The expiration date is March 31, 2019.
- Brand
Pharm D Solutions- Category
Drug
What to do — step by step
Check Product Label
Look for NDC 69699-1738-10 and lot number 10292018:21 on the product label.
Questions people ask
Is this product safe to use?
The product may not be sterile, which could cause infections if used improperly. Do not use this product until you contact the manufacturer.
What should I do if I have this product?
The recall does not specify a remedy, so contact Pharm D Solutions at 1-844-263-6843 for guidance.
How can I verify if I have the recalled product?
Check the NDC number 69699-1738-10 and lot number 10292018:21 on the product label.
Contact Pharm D Solutions
We’ve drafted a message you can send Pharm D Solutions to request your refund or repair — edit it as you like.
Subject: Recall D-0343-2019 — Pharm D Solutions Pharm D Solutions Hello, I own a Pharm D Solutions that is covered by recall D-0343-2019 from Pharm D Solutions. 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-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 qwen3:4b 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.