Recall Alert: Max Mobility/Permobil Removes All SpeedControl Dials Used with SmartDrive MX2+ Power Assist Devices
This recall involves removing certain devices from where they are used or sold. The FDA…
Fresenius Kabi Issues Voluntary Nationwide Recall of Three Lots of Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL Fill in a 2 mL Vial Due to Out-of-Specification Endotoxin Results in Certain Reserve Samples
Summary Company Announcement Date: November 06, 2025 FDA Publish Date: November 07, 2025 Product Type:…
Update: FDA Encourages the Public to Follow Established Choking Rescue Protocols – FDA Safety Communication
Español 简体中文 (Simplified Chinese) Tagalog Update: November 13, 2025The FDA has taken actions to address the marketing…
Alert: Siemens Healthineers Issues Correction for 3 Tesla MRI Systems
This recall involves correcting certain devices and does not involve removing them from where they…
Early Alert: Large Volume Pump Primary Administration Set Reverse Flow Issue from Fresenius Kabi
This Early Alert communication is part of the Communications Pilot to Enhance the Medical Device…
CDC Report Finds Sharp Rise in Dangerous Drug-Resistant Bacteria
A new report from the Centers for Disease Control and Prevention (CDC), published in the…