Zydus Lifesciences Limited – 9/5/2025

The Food and Drug Administration is advising consumers not to purchase or use HimGo, a product promoted and sold for sexual enhancement on various websites, including ebay.com, and possibly in some retail stores.

This page contains the DSARM roster, which lists the current members and the current number of vacancies for the committee.

Task Description Request Please post to the OII FOIA Electronic Reading Room
Record Date 09/23/2025
Short Title (70 char) Park Avenue Compounding. Saint Louis, MO. 483 issued 09/23/2025
FEI Number 1972829
Firm Name Park Avenue Compounding
Record Type 483
State MO
Establishment Type Outsourcing Facil

Task Description Request Please post to the OII FOIA Electronic Reading Room
Record Date 06/09/2022
Short Title (70 char) BlendHouse. Reading, PA. EIR issued 06/09/2022
FEI Number 3015728839
Firm Name BlendHouse
Record Type EIR
State PA
Establishment Type Manufacturer

FOR IMMEDIATE RELEASE – October 31, 2025 AUSTIN, TX – Otsuka ICU Medical LLC is issuing a voluntary recall to the user level, for a MISLABELLED lot of POTASSIUM CHLORIDE Inj. 20 mEq, NDC 0990-7077-14. The OVERWRAP label of lot 1030613, Expiration Date: 09-30-2026 may incorrectly identify the product

Task Description Request Please post to the 2017 Pharmacy Inspections and Related Records Web page
Record Date 03/23/2017
FEI Number 3013341563
Firm Name Fusion IV Pharmaceuticals Inc. dba Axia Pharmaceutical
Record Type 483
State CA
Establishment Type Producer of Sterile Drug Products