Vivus, Inc.: Drug Recall

Recall #D-0896-2023 · 06/23/2023

Class III: Low Risk

Recall Details

Recall Number
D-0896-2023
Classification
Class III
Product Type
Drug
Recalling Firm
Vivus, Inc.
Status
Ongoing
Date Initiated
06/23/2023
Location
Campbell, CA, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
4240 bottles

Reason for Recall

Failed Stability Specifications

Product Description

PANCREAZE (pancrelipase) Delayed-Release Capsules, 100-count bottles, Rx only, Rx only, Manufactured by VIVUS LLC, Campbell, CA 95008, UPC: N3 62541-401-10 5, NDC 62541-401-10,

Distribution Pattern

Nationwide within the United States

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.