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...
FDA alerts patients and healthcare professionals to Infusion Options’ voluntary recall due to quality issues
[6/21/2019] The U.S. Food and Drug Administration is alerting Healthcare professionals and patients of...
FDA alerts patients of McDaniel Life-Line’s voluntary recall of Indian Herb
Update [3/29/19] FDA is alerting health care professionals and patients of McDaniel Life-Line’s voluntarily...
FDA warns compounders not to use glutathione from Letco Medical to compound sterile drugs
Agency is aware of adverse events related to compounded glutathione injection [2/1/2019] FDA is warning...
FDA alerts consumers not to use two e-liquids sold by HelloCig Electronic Technology
[12/11/2018] The U.S. Food and Drug Administration is alerting consumers, particularly males, not to...
FDA alerts health care professionals and patients not to use drug products intended to be sterile from Promise Pharmacy
Compounded drugs were produced under poor sterile production practices in an inadequately designed processing...
FDA alerts health care professionals and patients not to use sterile drug products from Pharm D Solutions
[11/19/2018] The U.S. Food and Drug Administration is alerting Health care professionals and patients...
FDA alerts consumers of Kadesh Incorporation’s voluntary nationwide recall of Puriton Eye Relief Drops due to non-sterile production conditions
[11/8/2018] The Food and Drug Administration is alerting consumers about a voluntary recall of all lots...
FDA alerts patients and health care professionals that some EpiPen auto-injectors may not readily slide out of carrier tube
[11/2/2018] FDA is alerting patients, caregivers and Health care professionals that the labels attached...