FDA warns consumers of contaminated copycat eye drops
[1/31/2024] FDA is warning consumers not to purchase or use South Moon, Rebright or FivFivGo eye drops...
FDA announces shelf-life extension for naloxone nasal spray
Today, FDA is announcing that Emergent BioSolutions is extending the shelf-life of newly manufactured...
FDA requires updates to labeling for promethazine hydrochloride injection products
[12/27/2023] FDA is alerting health care professionals of labeling updates intended to further reduce...
FDA warns consumers not to purchase or use Neptune’s Fix or any tianeptine product due to serious risks
[11/21/2023] FDA is warning consumers to not purchase or use any Neptune’s Fix products, or any other...
FDA warns consumers of hidden drug ingredients in Dr. Ergin’s SugarMD Advanced Glucose Support
[11/3/2023] Consumers should not purchase or use Dr. Ergin’s SugarMD Advanced Glucose Support, a product...
FDA warns consumers not to purchase or use certain eye drops from several major brands due to risk of eye infection
[10/27/2023] FDA is warning consumers not to purchase and to immediately stop using 26 over-the-counter...
FDA is changing the therapeutic equivalence rating for Accord Healthcare Inc.’s generics of Prograf (tacrolimus) oral capsules
[9/18/2023] Based on new data, the U.S. Food and Drug Administration is changing the therapeutic equivalence...
FDA warns consumers not to purchase or use certain methylsulfonylmethane (MSM) eye drops due to contamination
[8/22/2023] FDA is warning consumers not to purchase and to immediately stop using Dr. Berne’s MSM...
FDA alerts consumers and pet owners of Silver Star Brand’s voluntary recall of homeopathic drug products
[10/4/2018] The Food and Drug Administration is alerting consumers and pet owners about a voluntary recall...
FDA warns consumers that Tydemy, a prescription oral contraceptive, may have reduced effectiveness
[August 1, 2023] FDA is warning consumers that two lots of Tydemy (drospirenone/ethinyl estradiol/levomefolate...
G-Supress DX Pediatric Cough Drops may have incorrect drug in packaging
En Español [5/22/2023] FDA is alerting consumers and pharmacies to not use or sell a specific lot of...
FDA warns consumers to not purchase or use Nose Slap and Soul Slap products marketed for alertness and energy boosting
[5/1/2023] FDA is warning consumers to not purchase or use Nose Slap and Soul Slap products, which are...
Infants at Risk for Aluminum Toxicity with Unapproved Potassium Phosphates Drug Product
FDA is warning Health care professionals and pharmacies to avoid using Hospira's unapproved potassium...
FDA warns consumers not to purchase or use EzriCare Artificial Tears due to potential contamination
Update [2/22/2023] FDA recommended that Global Pharma recall Delsam Pharma’s Artificial Eye Ointment,...
FDA alerts health care professionals of compatibility issues with prefilled glass syringes and certain Luer-activated valve (LAV) connectors
[11/22/2022] FDA is alerting health care professionals that certain Luer-activated valve (LAV) connectors...
FDA alerts health care professionals of risks to patients exposed to xylazine in illicit drugs
[11-8-2022] Health care professionals should be cautious of possible xylazine inclusion in fentanyl,...
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...