FDA recall Z-0089-2020

Product

CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840

Reason for recall

Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.

Distribution

Nationwide domestic distribution.

Key facts

Status

Terminated

Initiation date

2019-04-24

Report date

2019-10-16

Termination date

2020-04-03

Voluntary/Mandated

Voluntary: Firm initiated

Location

Williamston, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0089-2020