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ARROW INTERNATIONAL Inc. recalls Arrow Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic,
Recalled October 11, 2023 · FDA recall Z-0003-2024 · ARROW INTERNATIONAL
Hazard
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits. · FDA Class I
Units
380 units
Sold at
US
Description
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
Product
Arrow Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic, long-term greater than 30 days
Manufacturer(s)
ARROW INTERNATIONAL Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →