FDA Releases Guidelines on Regulation of Medical Software
The FDA has updated guidance on which medical devices are regulated by the agency.
FDA Issues Warning About Serious Security Flaws in Critical Medical Devices
The FDA warns manufacturers, healthcare providers, hospitals and patients that the “URGENT/11” security flaws may cause medical devices to malfunction.
FDA Takes Action to Reduce Risks Associated with Surgical Staplers
The FDA updates physicians about adverse events associated with surgical staplers and implantable surgical staples and provides recommendations for improving patient safety.
FDA Ban on Use of Powdered Gloves Is in Effect
Effective January 18, 2017, the FDA has banned the use of powdered gloves in healthcare. MLMIC recommends that all insureds protect their patients and ensure their practices are in compliance.