PlainRecalls
FDA Drug Low Class III Terminated

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

Reported: November 15, 2023 Initiated: October 26, 2023 #D-0093-2024

Product Description

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

Reason for Recall

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

Details

Recalling Firm
VistaPharm LLC
Units Affected
11,633 bottles
Distribution
Nationwide and Saudi Arabia
Location
Largo, FL

Frequently Asked Questions

What product 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.. Recalled by VistaPharm LLC. Units affected: 11,633 bottles.
Why was this product recalled?
Defective Container: The adaptor does not fit into the neck of the bottle after reconstitution with water.
Which agency issued this recall?
This recall was issued by the FDA Drug on November 15, 2023. Severity: Low. Recall number: D-0093-2024.