B Braun Medical Inc recalls CytoGuard Closed Luer Connector, Intravenous access 2 cartons of 50 units each (100 units per case)

Recall date

April 10, 2017

Source

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

Recall number

Z-2155-2017

FDA classification

Class II

Brand / firm

B Braun Medical Inc

Sold / distributed

United States Nationwide distribution

Why it was recalled

B. Braun is voluntarily recalling 13 lots of CytoGuard Closed Luer Connector due to a potential for some blisters to be punctured resulting in a compromised sterility barrier.

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

What was recalled

CytoGuard Closed Luer Connector, Intravenous access 2 cartons of 50 units each (100 units per case)