FDA warns consumers not to purchase or use Artri and Ortiga products,
en Español [7/3/2023] Since April 20, 2022, FDA learned that more than 30 additional consumers have experienced a serious health effect after using unapproved over-the-counter products with “Artri” or “Ortiga” in the product name. Reported harmful effects include...La FDA advierte a los consumidores
English Como apoyo a la seguridad pública, y debido a que algunos de estos productos aún pueden estar disponibles en el mercado, la FDA ha emitido cartas de advertencia el 28 de octubre de 2022 a Amazon, Walmart y Latin Foods Market por distribuir varios productos...FDA warns not to use products from FarmaKeio Compouding
[5/25/2022] FDA is alerting customers of North American Custom Laboratories LLC, doing business as FarmaKeio Superior Custom Compounding’s voluntary recall, initiated on April 5, 2022, of unexpired drug products that are intended to be sterile. This recall includes...Frequently requested or proactively posted drug-specific and other rec
4/1/2026Letter on Hemp-Derived Cannabidiol Products in Medical Research Models (PDF – 212 KB) 2/24/2025Product Resolution of Tirzepatide Injection Shortage and Supply Status (PDF – 1.103 KB)5/21/2024Drug Approval Package: JAYPIRCA11/9/2023First...All Drug Purchases Are
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