US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 14, 2022 (4 years ago)

PHENOBARBITAL Sodium Injection

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

Why it was recalled

Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.

What was recalled

PHENOBARBITAL Sodium Injection, USP, 130 mg/mL, packaged as a) 25 x 1 mL Vials per box (NDC 42494-416-25) and b) 3 x 1mL Vials per box (NDC 42494-416-03), Rx only, Manufactured for Cameron Pharmaceuticals, LLC.

Recalling firm
Vitae Enim Vitae Scientific, Inc.
NDC code
42494-416-25
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0744-2022

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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Class III · Low risk Terminated

Phenobarbital Elixir

Reason Does Not Meet USP or OTC Monograph: Product exceeds USP specification for alcohol content

Monarch PCM, LLC NDC 69367-172-16 D-0878-2022
Class II · Moderate risk Terminated

PHENOBARBITAL Sodium Injection

Reason Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.

Vitae Enim Vitae Scientific, Inc. NDC 42494-415-25 D-0743-2022
Class II · Moderate risk Terminated

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Reason CGMP Deviations: Intermittent exposure to temperature excursion during storage.

Cardinal Health Inc. NDC 13517-111-01 D-0470-2021
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Reason cGMP Deviations: Potential product contamination with Burkholderia cepacia (B.cepacia) and Ralstonia pickettii (R. pickettii).

Torrent Pharma Inc D-1365-2019
Class II · Moderate risk Terminated

Phenobarbital Oral Solution

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

Lohxa LLC NDC 70166-536-02 D-1131-2019