ARROW INTERNATIONAL Inc.: Medical Device Recall in 2023 - (Recall #: Z-0001-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product 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

Product Classification:

Class I

Date Initiated: August 10, 2023

Date Posted: October 11, 2023

Recall Number: Z-0001-2024

Event ID: 93014

Reason for Recall:

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

Status: Ongoing

Product Quantity: 1173 units

Code Information:

Batch/Lot number 33F23B0781

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated