VistaPharm LLC recalls Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured for: VistaPharm, Inc., Largo,…

Recall date

October 26, 2023

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0093-2024

FDA classification

Class III

Brand / firm

VistaPharm LLC

Sold / distributed

Nationwide and Saudi Arabia

Why it was recalled

Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

Mycophenolate Mofetil for Oral Suspension, USP, 200 mg/mL, Rx Only, bottle, Manufactured for: VistaPharm, Inc., Largo, FL 33771, USA, NDC#66689-307-08.