Arrow International Inc: Medical Device Recall in 2019 - (Recall #: Z-2556-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.

Product Classification:

Class II

Date Initiated: August 6, 2019

Date Posted: October 2, 2019

Recall Number: Z-2556-2019

Event ID: 83593

Reason for Recall:

Products may contain the incorrect banner card within the kit

Status: Terminated

Product Quantity: 231 units

Code Information:

Lot Number: 13F18H0499

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated