ARROW INTERNATIONAL Inc. recalls Arrow ErgoPack, Pressure Injectable Two-Lumen PICC pre-loaded with Arrow VPS Stylet, REF CDC-35552-VPS; Catheter: Percut

Recalled September 27, 2023 · FDA recall Z-2591-2023 · 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

177 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 Two-Lumen PICC pre-loaded with Arrow VPS Stylet, REF CDC-35552-VPS; Catheter: Percutaneous, implanted, long-term intravascular catheter

Manufacturer(s)

ARROW INTERNATIONAL Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →