News and Updates
Infusion Pump Administration Set Recall: Fresenius Kabi USA Removes Certain Ivenix Large Volume Pump Primary Administration Sets
This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or
Disruption in Availability of BD BACTEC Blood Culture Media Bottles – Letter to Health Care Providers
The U.S. Food and Drug Administration (FDA) is aware that the U.S. is experiencing interruptions in the supply of BD BACTEC blood culture media bottles because of recent supplier issues.
Fresenius Medical Care Recalls Sanxin Single-Use Syringes for Leakages
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Device Use The Fresenius
Do Not Use Certain Brands of Saline and Sterile Water Medical Products by Nurse Assist Because They May Not Be Sterile
The U.S. Food and Drug Administration (FDA) is warning consumers, health care providers, and health care facilities not to use recalled saline (0.9% sodium chloride) and sterile water medical products
Exela Pharma Sciences, LLC Issues Voluntary Nationwide Recall
Exela Pharma Sciences, LLC, (Exela) is voluntarily recalling the products listed in the link below to the consumer level. Particulate matter identified as silicone was observed during routine inspection of
NEW CDC Toolkits to Prepare for Flu, COVID-19, and RSV
CDC recently released a new Resources to Prepare for Flu, COVID-19, and RSVwebpage which provides toolkits and resources for various communities on preparing for the flu, COVID-19, and respiratory syncytial
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