Medical Product Recalls
FDA Enforcement Report is published weekly by the Food and Drug Administration, Department of Health and Human Services. It contains information on actions taken in connection with agency Regulatory activities.
MedWatch, The FDA Safety Information and Adverse Event Reporting Program, serves both healthcare professionals and the medical product-using public. Information is provided on safety issues involving medical products, including prescription and over-the-counter drugs, biologics, medical and radiation-emitting devices, and special nutritional products (e.g., medical foods, dietary supplements and infant formulas).
Note: TTUHSC El Paso Safety Services publishes this information, as is, from the FDA. Please contact the manufacturer for more information.
9/1/15BD Plastic Sterile Syringe Recall: Decreased potency when drugs are compounded or repackaged and stored in these syringes.