Class II · Moderate risk Ongoing
Nandrolone Decanoate 200mg/mL
Reason Lack of Assurance of Sterility
Nandrolone 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 200 mg/ml Injection, 10 mL and 20 mL vials, Rx, B & B Health Mart Pharmacy, Bellflower, CA
- Recalling firm
- Pacific Healthcare, Inc dba B&B Pharmacy
- Origin
- CA, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0166-2016
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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