Arrow International Inc: Medical Device Recall in 2016 - (Recall #: Z-2911-2016)

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:

Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is intended for use in removing arterial emboli.

Product Classification:

Class II

Date Initiated: July 7, 2016

Date Posted: October 12, 2016

Recall Number: Z-2911-2016

Event ID: 75014

Reason for Recall:

Arrow is recalling due to incorrect labeling of products.

Status: Terminated

Product Quantity: 2,425 catheters

Code Information:

Lot/Batch 14F15H0292, 14F15J0139, 14F15A0174, CF3016366, 14F14E0300, 14F15G0349, 14F15H0261, CF2079921, 14F15J0363, 14F14J0155, 14F15F0406, 14F15E0263, 14F15H0258, 14F15H0251, 14F15G0347. CF2125865, 14F15D0197, 14F15H0025, 14F15H0332, 14F15B0244, 14F15G0348

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated