- Main Street Family Pharmacy in Tennessee: FDA Alerts Health Care Providers of Adverse Reactions Associated with Steroid Injections
- Cook Medical, Inc Zilver PTX Drug-Eluting Peripheral Stent: Class 1 Recall - Complaints of Delivery System Tip Separation
- Methotrexate Sodium, USP Injectable Vials by Sandoz US: Recall - Particulate Matter In Vials
- Abbott Diabetes Care: Class 1 Recall - FreeStyle InsuLinx Blood Glucose Meters - Risk of Incorrect Test Result
- All Sterile Drug Products Made and Distributed By NuVision Pharmacy Dallas Facility: Recall - Lack Of Sterility Assurance
- Compounded Prescription Therapies By Pentec Health Inc.: Recall - Lack Of Sterility Assurance
- Zolpidem Containing Products: Drug Safety Communication - FDA Requires Lower Recommended Doses
- Atriphen dietary supplement (Xymogen brand): Recall - Potential Allergic Reaction Due to Milk and Soy
- The Compounding Shop: FDA News Release - Lack of Sterility Assurance of Drug Products
- SexVoltz, Velextra, and Amerect by Beomonstar Products: Recall - Undeclared Drug Ingredient
- Bullet Proof: Public Notification - Undeclared Drug Ingredient
- Lightning Rod Capsules: Recall - Undeclared Drug Ingredient
- Maquet SERVO-i Ventilator Battery Module: Class 1 Recall - Battery Run Time Shorter Than Expected
- Medtronic: Class 1 Recall - Medtronic Deep Brain Stimulation Lead Kit and Activa Dystonia HDE Kit
- Covidien Surgical Stapler Reloads: FDA Safety Communication - Devices Stolen Before They Were Sterilized
FDA Medwatch
