Arrow International Inc: Medical Device Recall in 2021 - (Recall #: Z-1106-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Arrow AGB+ Multi-Lumen CVC Kit 7Fr 3 Lumen- Intended for venous access to the central circulation by the way of the femoral, jugular, or subclavian veins. Product Code: CDC-45703-1A

Product Classification:

Class II

Date Initiated: January 6, 2021

Date Posted: February 17, 2021

Recall Number: Z-1106-2021

Event ID: 87092

Reason for Recall:

The lidstock / information card on the kits correctly states the product code as CDC-45703-1A. The banner card on the side of the kit may incorrectly state the product code as CDC-15703-1A and not identify the product as a coated ARROWg+ard Blue PLUS (AGB+) antimicrobial catheter which may cause a minor delay during use and placement of a coated catheter in patients with known sensitivity to chlorohexidine, silver sulfadiazine or sulfa could result in an allergic reaction

Status: Terminated

Product Quantity: 1,705 eaches

Code Information:

Lot Code: 13F20E0173

Distribution Pattern:

US Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated