ARROW INTERNATIONAL Inc.: Medical Device Recall in 2023 - (Recall #: Z-2590-2023)

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 One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intravascular

Product Classification:

Class II

Date Initiated: August 10, 2023

Date Posted: September 27, 2023

Recall Number: Z-2590-2023

Event ID: 92850

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: 190 units

Code Information:

Batch/Lot number 13F22J0617

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated