Arrow International Inc: Medical Device Recall in 2014 - (Recall #: Z-0114-2015)

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:

ASK-05501-AFH1, Lot Number 23F13K0969 Anesthesia Conduction Catheter, Epidural Anesthesia Kit

Product Classification:

Class II

Date Initiated: September 15, 2014

Date Posted: October 29, 2014

Recall Number: Z-0114-2015

Event ID: 69256

Reason for Recall:

Arrow International, Inc. is notifying customers that lot 23F13K0969 of product code ASK-05501-AFH1 contains an incorrect component. The lidstock indicates that the kit contains one Syringe, 10mL, Luer-Slip Loss of Resistance, Glass but contains one Syringe, 10mL, Luer-Lock Loss of Resistance, Glass.

Status: Terminated

Product Quantity: 300

Code Information:

Catalog No. ASK-05501-AFH1 Lot Number 23F13K0969

Distribution Pattern:

US Distribution in Utah only.

Voluntary or Mandated:

Voluntary: Firm initiated