US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jan 2, 2019 (8 years ago)

Hydroxyprogesterone liquid, 250mg/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

Hydroxyprogesterone liquid, 250mg/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-0396-2019

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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