Arrow International Inc: Medical Device Recall in 2014 - (Recall #: Z-0076-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Multi-Lumen Central Venous Catheterization Kit

Product Classification:

Class II

Date Initiated: September 18, 2014

Date Posted: October 22, 2014

Recall Number: Z-0076-2015

Event ID: 69290

Reason for Recall:

Arrow International, Inc. has initiated a voluntary recall for product code AK- 12703, lot number RF3039028 because the label on the outer corrugate is labeled with the incorrect expiration date. All kits packaged within the corrugate are correctly labeled. There is no risk to the patient as the kits within the corrugate are labeled with the correct expiration date.

Status: Terminated

Product Quantity: 65

Code Information:

Catolog No - AK-12703 lot number RF3039028

Distribution Pattern:

US Distribution including the states of MD, NC , LA , IN , OH, KY, CA , PA , NY and NV.

Voluntary or Mandated:

Voluntary: Firm initiated