Arrow International Inc: Medical Device Recall in 2016 - (Recall #: Z-2741-2016)

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:

Radial Artery Catheterization Kit with Sharps Safety Features Permits access to the peripheral arterial circulation. The safety feature is intended to help minimize the risk of sharps injuries when using the device.

Product Classification:

Class II

Date Initiated: August 8, 2016

Date Posted: September 14, 2016

Recall Number: Z-2741-2016

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