Arrow International Inc: Medical Device Recall in 2017 - (Recall #: Z-2699-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Arrow Glide Thru Peel-Away Sheath/Dilator Introducer

Product Classification:

Class II

Date Initiated: June 12, 2017

Date Posted: July 19, 2017

Recall Number: Z-2699-2017

Event ID: 77604

Reason for Recall:

Arrow is recalling additional lots that were identified as part of an active recall. Arrow is recalling the affected product due to the possibility that the catheter peel-away component hub tabs may prematurely detach when the practitioner begins to peel apart the sheath body from the catheter.

Status: Terminated

Product Quantity: 9,037 units in the U.S. and 4,505 Internationally

Code Information:

Device Listing # D184260 Material # PL-01055

Distribution Pattern:

Distributed to SC, AL, NJ, IN, MA, GA, CA, PA, AZ, VA , WA and Bangkok

Voluntary or Mandated:

Voluntary: Firm initiated