ARROW INTERNATIONAL Inc.: Medical Device Recall in 2023 - (Recall #: Z-0002-2024)

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 Complete, Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC, REF CDC-42854- PCN1A; catheter, intravascular, therapeutic, long-term greater than 30 days

Product Classification:

Class I

Date Initiated: August 10, 2023

Date Posted: October 11, 2023

Recall Number: Z-0002-2024

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: 180 units

Code Information:

Batch/Lot number 33F23B0723

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated