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Arrow International Inc recalls Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arro
Recalled October 2, 2019 · FDA recall Z-2556-2019 · Arrow International
Hazard
Products may contain the incorrect banner card within the kit · FDA Class II
Units
231 units
Sold at
US Nationwide distribution.
Description
Products may contain the incorrect banner card within the kit
Product
Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.
Manufacturer(s)
Arrow International Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →