US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 20, 2023 (3 years ago)

Tiglutik (riluzole) Oral Suspension 50 mg/10 mL (5 mg/mL), 600 mL (two bottles/300 mL…

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

Why it was recalled

Failed Viscosity Specifications: Out-of-specification test results for viscosity

What was recalled

Tiglutik (riluzole) Oral Suspension 50 mg/10 mL (5 mg/mL), 600 mL (two bottles/300 mL each), RX only, Manufactured for ITF Pharma, Inc., Berwyn, PA 19312 USA NDC:70726-0303-1 (carton) and 70726-0303-2 (bottle)

Recalling firm
Itf Pharma INC
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0115-2024

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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