Class II · Moderate risk Ongoing
Nandrolone Decanoate 200mg/mL
Reason Lack of Assurance of Sterility
Nandrolone Decanoate Injectable
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Assurance of Sterility; FDA inspectional findings resulted in concerns associated with quality control procedures that impacted sterility assurance
What was recalled
Nandrolone Decanoate Injectable, compounded by Pallimed Solutions Pharmacy, Woburn, MA
- Recalling firm
- Pallimed Solutions
- Origin
- MA, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-873-2013
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Nandrolone recalls
See all
Class III · Low risk Terminated
Nandrolone Decanoate
Reason Subpotent Drug
Class III · Low risk Terminated
Nandrolone Decanoate
Reason Subpotent Drug
Class III · Low risk Terminated
Nandrolone Decanoate
Reason Subpotent Drug
Class III · Low risk Terminated
Nandrolone Decanoate
Reason Subpotent Drug
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