FDA recall D-0208-2025

Product

Venlafaxine Extended-Release Tablets, 150mg, Rx only, 90 Tablets, Manufactured by Appco Pharma. LLC, NDC 43598-943-90.

Reason for recall

Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet

Distribution

Nationwide USA.

Key facts

Status

Completed

Initiation date

2025-01-16

Report date

2025-01-29

Voluntary/Mandated

Voluntary: Firm initiated

Location

Piscataway, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0208-2025