Testosteron Cypionate liquid 200mg/ml, RX, glass vial
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of sterility assurance.
What was recalled
Testosteron Cypionate liquid 200mg/ml, RX, glass vial
- Recalling firm
- Hiers Enterprises, LLC dba Northwest Compounding Pharmacy
- Origin
- OR, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0401-2019
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.
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