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ARROW INTERNATIONAL Inc. recalls Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intravascular
Recalled September 27, 2023 · FDA recall Z-2590-2023 · 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 II
Units
190 units
Sold at
US Nationwide distribution.
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 ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intravascular
Manufacturer(s)
ARROW INTERNATIONAL Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →