Centurion Medical Products Corporation recalls CENTRAL LINE BUNDLE ECVC6375

Recall date

April 24, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0097-2020

FDA classification

Class II

Brand / firm

Centurion Medical Products Corporation

Sold / distributed

Nationwide domestic distribution.

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

CENTRAL LINE BUNDLE ECVC6375