Arrow International Inc: Medical Device Recall in 2013 - (Recall #: Z-1965-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Arrow International, Inc. Two-Lumen CVC Kit with Blue Flex Tip Catheter. The multiple lumen catheter permits venous access to the central circulation of patients.

Product Classification:

Class II

Date Initiated: July 31, 2013

Date Posted: August 21, 2013

Recall Number: Z-1965-2013

Event ID: 65829

Reason for Recall:

Arrow is recalling the product due to a labeling inconsistency. One portion of the lidstock states the kit contains a 3-Lumen catheter while the rest of the lidstock correctly identifies the catheter as 2-Lumen.

Status: Terminated

Product Quantity: 156

Code Information:

Catalog # AK-17702-CDC, lot # RF2083258

Distribution Pattern:

AL, PA, CT, NC, VA, KS, RI, AZ, NJ, and IL.

Voluntary or Mandated:

Voluntary: Firm initiated