US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 20, 2016 (10 years ago)

Placebo for Prednisolone Acetate 1%, Oph Suspension, 10 mL Dropper Bottle, Compounded by…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters

What was recalled

Placebo for Prednisolone Acetate 1%, Oph Suspension, 10 mL Dropper Bottle, Compounded by Leiter's Compounding, San Jose, CA

Recalling firm
Leiter's Compounding
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0017-2017

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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