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

Recalled November 15, 2023 · FDA recall D-0093-2024 · VistaPharm

Hazard

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

Units

11,633 bottles

Sold at

Nationwide and Saudi Arabia

Description

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

Product

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

Manufacturer(s)

VistaPharm LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →