Arrow International Inc: Medical Device Recall in 2018 - (Recall #: Z-1194-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

ARROW ENDURANCE" Extended Dwell Peripheral Catheter System, Catalog Numbers: EDC-00820 & EDC-00820-B

Product Classification:

Class II

Date Initiated: December 15, 2017

Date Posted: April 4, 2018

Recall Number: Z-1194-2018

Event ID: 79474

Reason for Recall:

Certain lots of peripheral catheter systems may be missing the safety latch, intended to minimize the risk of sharps injuries.

Status: Terminated

Product Quantity: 305

Code Information:

Catalog Number: EDC-00820, Lot: 14X17C0039 (Expires February 2019); Catalog Number: EDC-00820-B, Lot: 13F17F0120 (Expires May 2019)

Distribution Pattern:

Distributed in the following U.S. states: CO, FL, IL, NC, PA, SC, and TX.

Voluntary or Mandated:

Voluntary: Firm initiated