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

Recalled April 4, 2018 · FDA recall Z-1194-2018 · Arrow International

Hazard

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

Units

305

Sold at

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

Description

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

Product

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

Manufacturer(s)

Arrow International Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →