The Knowledge Shelf

Task Description Request Please post to the OII FOIA Electronic Reading Room
Record Date 11/19/2020
Short Title (70 char) Howard I. Schwartz, M.D. Hollywood, FL. EIR issued 11/19/2020
FEI Number 1000525885
Firm Name Howard I. Schwartz, M.D.
Record Type EIR
State FL
Establishment Type Clinical Invest

Task Description Request Please post to the OII FOIA Electronic Reading Room
Record Date 11/17/2020
Short Title (70 char) Jose F. Cardona, M.D. Hialeah, FL. EIR issued 11/17/2020
FEI Number 3008031588
Firm Name Jose F. Cardona, M.D.
Record Type EIR
State FL
Establishment Type Clinical Investigations

January 12, 2026, VH Foods Inc. DBA Outside The Breadbox of Colorado Springs, CO is recalling its 8 ounce packages of “Bread Crumbs” because they may contain undeclared egg and milk

Novel Drug Approvals for 2026

The U.S. Food and Drug Administration today approved the Zycubo (copper histidinate) injection as the first treatment for Menkes disease in pediatric patients.

Raleigh, North Carolina (January 12, 2026) — Spring & Mulberry is voluntarily recalling lot #025255 of its Mint Leaf Date Sweetened Chocolate Bar (2.1 oz) due to possible contamination with Salmonella.

Karison Foods & Snacks Inc of Port Washington, NY 11050 is recalling 12 oz containers of ‘PANJIRI’, ‘ALSI PINNI’, ‘PUNJABI PINNI’, ‘BESAN LADDOO’, and ‘NO SUGAR ADDED BESAN LADDOO’ due to undeclared milk allergen

[Phoenix, Arizona] – [12/22/25] – Modern Warrior is voluntarily recalling all lots of Modern Warrior Ready, a dietary supplement sold directly to consumers, after regulatory testing identified the presence of undeclared ingredients, including tianeptine, 1,4-DMAA, and aniracetam..Tianeptine can c

01/07/2026 – HerbsForever LLC of Los Angeles, California is recalling 45 units of the product “Hingwastik Churna” and 45 units of “Gastro Care” dietary supplements because they may contain undeclared wheat. People who have a wheat allergy run a risk of serious or life-threatening allergic reactions

Rosemead, CA, ANTHONY TRINH, 123herbals LLC is voluntarily recalling all lots of Silintan capsules to the consumer level. FDA analysis has found the product to be tainted with meloxicam. Meloxicam, is an approved Nonsteroidal Anti-Inflammatory Drug, (NSAID) indicated for management of osteoarthritis