US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 25, 2019 (7 years ago)

Phenobarbital Oral Solution, USP 20 mg/5mL, unit dose cup, Rx Only, Rpkg. By.Lohxa…

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

Why it was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date - the label contains an incorrect Exp Date.

What was recalled

Phenobarbital Oral Solution, USP 20 mg/5mL, unit dose cup, Rx Only, Rpkg. By.Lohxa Worcester, MA 01608 NDC 70166-536-02

Recalling firm
Lohxa LLC
NDC code
70166-536-02
Origin
MA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1131-2019

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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