FDA recall Z-1290-2022

ARROW INTERNATIONAL Inc. · Class II · device

Product

Arrow Three-Lumen CVC

Reason for recall

Gravity flow rates on the affected product lidstock are incorrect.

Distribution

US Nationwide distribution in the states of Florida.

Key facts

Status
Terminated
Initiation date
2022-05-05
Report date
2022-07-06
Termination date
2024-09-04
Voluntary/Mandated
Voluntary: Firm initiated
Location
Morrisville, NC, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1290-2022