FDA issues Class I recall of venous access, catheter kits

Dec 19, 2022 - 03:20 PM
FDA-device-recall

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.

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