Arrow International Inc: Medical Device Recall in 2014 - (Recall #: Z-1507-2014)

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:

Arrowgard Blue Plus Antimicrobial Multi-lumen Central Venous Catheter, catalogue number AK-45854-CDC.

Product Classification:

Class II

Date Initiated: July 17, 2013

Date Posted: April 30, 2014

Recall Number: Z-1507-2014

Event ID: 67834

Reason for Recall:

Arrow is recalling the Arrowgard Blue Plus Antimicrobial Multi-lumen Central Venous Catheter due to a labeling inconsistency. One portion of the lidstock states that the kit contains 8.5FR x 16CM catheter, while the rest of the lidstock correctly identifies the catheter as 8.5FR x 20CM

Status: Terminated

Product Quantity: 170

Code Information:

lot RF2110924

Distribution Pattern:

US Distribution including the states of IA, OR, WV, MI, AZ, IL, PA, GA, DE, NC, LA, and VA.

Voluntary or Mandated:

Voluntary: Firm initiated