Rymed Technologies, LLC recalls InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, Single Use Products are intended for single…

Recall date

January 5, 2016

Source

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

Recall number

Z-0675-2016

FDA classification

Class II

Brand / firm

Rymed Technologies, LLC

Sold / distributed

US Nationwide Distribution.

Why it was recalled

Potential for the female luer component of the InVision-Plus IV connector to crack during use.

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

What was recalled

InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, Single Use Products are intended for single patient use in intravenous and blood administration sets without the need for needles, thus eliminating the potential for needle-stick injuries during use.