FDA recall Z-0690-2018

Arrow International Inc · Class II · device

Product

ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet

Reason for recall

The kit may contain an incorrect catheter component. Kits that should contain a 40cm catheter may contain a 55cm catheter.

Distribution

AZ, CA, GA, MA, MO, NY, VA

Key facts

Status
Terminated
Initiation date
2017-10-17
Report date
2018-02-28
Termination date
2020-04-21
Voluntary/Mandated
Voluntary: Firm initiated
Location
Reading, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0690-2018