FDA alerts patients, caregivers, and health care providers of cross-compatibility issues with autoinjector devices that are optional for use with glatiramer acetate injection
[8/18/2022] FDA is alerting patients, caregivers, and health care professionals that autoinjector devices...
Bosentan REMS requirements will change June 27, 2022
On April 29, 2022, the U.S. Food and Drug Administration approved a modification to the Bosentan Risk...
FDA alerts customers to voluntary recall of compounded drugs due to sterility issues by Drug Depot, LLC, dba APS Pharmacy
[4/26/2022] FDA is alerting patients, health care professionals, veterinarians, and animal owners/caretakers...
FDA warns consumers not to purchase or use Artri and Ortiga products, which may contain hidden drug ingredients
en Español [7/3/2023] Since April 20, 2022, FDA learned that more than 30 additional consumers have...
FDA warns patients and health care professionals not to use sterile products from North American Custom Laboratories LLC, dba FarmaKeio Superior Custom Compounding
[5/25/2022] FDA is alerting customers of North American Custom Laboratories LLC, doing business as FarmaKeio...
FDA alerts patients and health care professionals not to use compounded products intended to be sterile from Prescription Labs Inc. dba Greenpark Compounding Pharmacy
[9/29/2021] Update: FDA is alerting veterinarians and animal owners/caretakers not to use compounded...
FDA alerts patients and health care professionals about clinical trial results showing an increased risk of death associated with Pepaxto (melphalan flufenamide)
[7/28/2021] FDA is alerting patients and Health care professionals that a clinical trial (OCEAN, Study...
FDA advises health care professionals not to use ChloraPrep 3 mL applicators manufactured by BD (Becton, Dickinson and Company)
Update [3/25/2021] FDA is alerting health care professionals of BD’s voluntary recall expansion of...
FDA Alerts Healthcare Professionals About the Risk of Medication Errors with Tranexamic Acid Injection Resulting in Inadvertent Intrathecal (Spinal) Injection
[12/3/2020] The U.S. Food and Drug Administration is alerting Health care professionals about the risk...
FDA updates vinca alkaloid labeling for preparation in intravenous infusion bags only
[4/21/22] FDA worked with drug application holders to remove instructions for preparation of vinca alkaloids...
FDA Alerts of Perrigo's voluntary albuterol inhaler recall
[9/21/2020] The U.S. Food and Drug Administration is alerting health care professionals and patients...
FDA alerts health care professionals and oncology clinical investigators about efficacy and potential safety concerns with atezolizumab in combination with paclitaxel for treatment of breast cancer
[9/08/2020] FDA is alerting health care professionals, oncology clinical investigators, and patients...
FDA advises consumers not to use goldenseal root powder distributed by Maison Terre
Update [8/19/2020] FDA is alerting consumers and health care professionals to Maison Terre’s voluntary...
FDA updates on hand sanitizers consumers should not use
Need help now? Call 9-1-1 if the person is unconscious or has trouble breathing. Call Poison Help at...
FDA advises consumers not to use hand sanitizer products manufactured by Eskbiochem
Spanish version Update [6/29/2020] FDA is alerting consumers of Saniderm Products and UVT Inc.’s voluntary...
FDA alerts patients and health care professionals of Amneal and Impax Laboratories epinephrine auto-injector device malfunctions
[6/1/2020] FDA is alerting patients, caregivers and health care professionals to immediately inspect...
FDA alerts patients and health care professionals of EpiPen auto-injector errors related to device malfunctions and user administration
Update [4/9/2020] FDA is notifying patients and caregivers that EpiPens are not being recalled at this...
FDA advises consumers not to use Rompe Pecho cough syrup
en Español [10/11/2019] FDA advises consumers not to use Rompe Pecho EX and Rompe Pecho CF cough syrups...
FDA advises patients not to use Herbal Doctor Remedies’ medicines
[4/1/2020] FDA reminds patients not to use any drugs manufactured by Herbal Doctor Remedies, Monterey...
FDA announces Pacifico National Inc.’s, dba AmEx Pharmacy, voluntary recall of all sterile compounded drugs
Update [9/9/2019] FDA is alerting patients and Health care professionals of Pacifico National Inc.’s,...
FDA alerts consumers not to use Kratom NC’s products
[6/25/2019] FDA is warning consumers not to use products marketed by Kratom NC, of Wilmington, North...