FDA Enforcement Class I Ongoing

Arrow ErgoPack, Pressure Injectable Arrowg+ard Blue Advance Two-Lumen PICC pre-loaded with Arrow VPS Precision Stylet, REF CDC-45552-VPS2; Catheter: Percutaneous Implanted Long-Term Intravascular Catheter Stylet: Diagnostic Intravascular Catheter

Recall: Z-0001-2024 · Reported October 11, 2023

Enforcement

Recall Number
Z-0001-2024
Event ID
93014
Classification
Class I
Status
Ongoing
Product Type
Devices
Firm
ARROW INTERNATIONAL Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
October 11, 2023
Initiation Date
August 10, 2023
Classification Date
October 4, 2023
Address
3015 Carrington Mill Blvd, N/A, Morrisville, NC, 27560-5437, United States

Description

Arrow ErgoPack, Pressure Injectable Arrowg+ard Blue Advance Two-Lumen PICC pre-loaded with Arrow VPS Precision Stylet, REF CDC-45552-VPS2; Catheter: Percutaneous Implanted Long-Term Intravascular Catheter Stylet: Diagnostic Intravascular Catheter

Reason

This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.

Code Info

Batch/Lot number 33F23B0781

Distribution

US

Quantity

1173 units