FDA recall Z-2556-2019

Product

Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.

Reason for recall

Products may contain the incorrect banner card within the kit

Distribution

US Nationwide distribution.

Key facts

Status

Terminated

Initiation date

2019-08-06

Report date

2019-10-02

Termination date

2020-09-29

Voluntary/Mandated

Voluntary: Firm initiated

Location

Reading, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2556-2019