Arrow International Inc: Medical Device Recall in 2016 - (Recall #: Z-2201-2016)

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:

Femoral Arterial Line Catheterization Kit with Sharps Safety Features 510K 810675, product code DQX, Device Listing D025180 Material ASK-04018-VUH Product Usage: The Arrow arterial catheterization device permits access to the peripheral arterial circulation.

Product Classification:

Class II

Date Initiated: June 2, 2016

Date Posted: July 20, 2016

Recall Number: Z-2201-2016

Event ID: 74489

Reason for Recall:

Labeling error. Some shipping cartons labeled as ASK-04018-VUH contained ASK-04020-VUH kits; and some shipping cartons labeled as ASK-04020-VUH contained ASK-04018-VUH kits.

Status: Terminated

Product Quantity: 50 units in total

Code Information:

Lot/Batch Numbers: 23F14M0829, 23F14M0986

Distribution Pattern:

US distribution in the states of TN and KY.

Voluntary or Mandated:

Voluntary: Firm initiated