Arrow International Inc: Medical Device Recall in 2016 - (Recall #: Z-2740-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Arterial Line Catheterization Kit with Sharps Safety Features Permits access to the peripheral arterial circulation or to other small vessels.

Product Classification:

Class II

Date Initiated: August 8, 2016

Date Posted: September 14, 2016

Recall Number: Z-2740-2016

Event ID: 74986

Reason for Recall:

Shipping carton labeling error.

Status: Terminated

Product Quantity: 690 kits

Code Information:

Device Listing # D025180

Distribution Pattern:

Nationwide Distribution to OH, IN, TN, NC, and KY.

Voluntary or Mandated:

Voluntary: Firm initiated