PlainRecalls
FDA Drug Moderate Class II Terminated

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)

Reported: November 29, 2023 Initiated: October 20, 2023 #D-0115-2024

Product Description

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)

Reason for Recall

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

Details

Recalling Firm
ITF PHARMA INC
Units Affected
1,792 bottles
Distribution
Distributed to one distributor in TN who may have further distributed.
Location
Berwyn, PA

Frequently Asked Questions

What product 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). Recalled by ITF PHARMA INC. Units affected: 1,792 bottles.
Why was this product recalled?
Failed Viscosity Specifications: Out-of-specification test results for viscosity
Which agency issued this recall?
This recall was issued by the FDA Drug on November 29, 2023. Severity: Moderate. Recall number: D-0115-2024.