Healthcare innovation

FDA issues Class I recall of venous…


FDA issues Class I recall of venous…

The U.S. Food & Drug Administration has issued a Class I recall, the most serious type of recall, for the Arrow MAC Two-Lumen Central Venous Access Kits and Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen Central Venous Catheter Kits. Inadequate connections between the top and bottom housings could result in leakage, infection, serious injuries or death. No injuries or deaths have been reported.


Leave your thought here

Your email address will not be published. Required fields are marked *