Fagron recalls 500g Nandrolone Decanoate for prescription compounding due to subpotent drug risk. Affected units have specific NDC and lot numbers. Contact for return instructions.
Subpotent Drug
Fagron is recalling prescription-compounded Nandrolone Decanoate 500g products because they may be subpotent. This means the medication might not work as intended for patients who need it.
Subpotent drugs have lower active ingredient levels than intended, which could lead to ineffective treatment. This is a risk for patients relying on the medication for medical purposes.
Prescription compounding pharmacies and patients using this specific medication under a doctor's order. Those with the listed NDC and lot numbers are most at risk.
Check for the NDC code 51552-1564-05 and lot numbers 18H02-U02-044978, 18L12-U02-050018, or 18L12-U02-000952. Products were sold with expiration dates up to October 31, 2022, or September 2023.
Verify the NDC code and lot numbers listed in the recall notice to confirm if your product is affected.
The recall states the product may be subpotent, meaning it might not work as intended. Do not use if you have the listed NDC and lot numbers.
Check for the NDC code 51552-1564-05 and lot numbers 18H02-U02-044978, 18L12-U02-050018, or 18L12-U02-000952.
The recall does not specify a remedy, so contact Fagron directly for guidance on next steps.
We’ve drafted a message you can send Fagron to request your refund or repair — edit it as you like.
Subject: Recall D-0863-2022 — Fagron Fagron Hello, I own a Fagron that is covered by recall D-0863-2022 from Fagron. 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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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.
