Class II · Moderate risk Ongoing
Nandrolone Decanoate 200mg/mL
Reason Lack of Assurance of Sterility
Nandrolone Decanoate 200 mg/ml Injection
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
What was recalled
Nandrolone Decanoate 200 mg/ml Injection, ml Multi-Dose Vial, Sterile, Room Temperature, The Compounding Pharmacy of America, Knoxville, TN
- Recalling firm
- The Compounding Pharmacy of America
- Origin
- TN, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1616-2015
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
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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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