Rymed Technologies, LLC recalls InVision-Plus CS Needleless IV Connector, Catalog Number RYM-7001. Disposable, Single Use. Products are intended for si…

Recall date

January 5, 2016

Source

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

Recall number

Z-0676-2016

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 CS Needleless IV Connector, Catalog Number RYM-7001. 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.