FDA Enforcement Class II Terminated

CVC BUNDLE VANTEX 7F, 3L, 20CM ECVC6065

Recall: Z-0094-2020 · Reported October 16, 2019

Enforcement

Recall Number
Z-0094-2020
Event ID
83584
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Centurion Medical Products Corporation
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
October 16, 2019
Initiation Date
April 24, 2019
Classification Date
October 9, 2019
Termination Date
April 3, 2020
Address
100 Centurion Way, N/A, Williamston, MI, 48895-9086, United States

Description

CVC BUNDLE VANTEX 7F, 3L, 20CM ECVC6065

Reason

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.

Code Info

2018082450 2018091850 2018121850 2018122150 2019011550 2019012450 2019013050

Distribution

Nationwide domestic distribution.

Quantity

181965 total