Arrow International Inc: Medical Device Recall in 2019 - (Recall #: Z-0723-2019)

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 CVC 2 Lumen, Pediatric Two-Lumen Central Venous Cauterization Set with Blue FlexTip Catheter, 4 Fr 2 Lumen 5cm, Reference # CS-12402 The Arrow CVC is intended to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring central venous access, including, but not limited to the following: " Lack of usable peripheral IV sites " Central venous pressure monitoring " Total parenteral nutrition (TPN) " Infusions of fluids, medications, or chemotherapy " Frequent blood sampling or receiving blood transfusions/blood products

Product Classification:

Class II

Date Initiated: November 14, 2018

Date Posted: January 23, 2019

Recall Number: Z-0723-2019

Event ID: 81665

Reason for Recall:

The lidstock states the incorrect priming volume and flow rates.

Status: Terminated

Product Quantity: 15 in the US

Code Information:

Lots 14F18F0336 & 14F18E0121

Distribution Pattern:

Worldwide distribution: US (nationwide) distribution to state of: FL and to countries of: Argentina, Canada, Chile, Columbia, Costa Rica, Dominican Republic, Ecuador, and Peru.

Voluntary or Mandated:

Voluntary: Firm initiated