Metrex Research, LLC. recalls CaviWipes1 Extra Large, Part No. 13-5150 The brand name of the device is CaviWipes1 Extra Large, a surface disinfectant…

Recall date

January 20, 2017

Source

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

Recall number

Z-1402-2017

FDA classification

Class II

Brand / firm

Metrex Research, LLC.

Sold / distributed

Nationwide Distribution to PA, FL, IL, MN, TX, AL, NY

Why it was recalled

Metrex is recalling the CaviWipes Extra Large because they may have been contaminated during the packaging process.

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

What was recalled

CaviWipes1 Extra Large, Part No. 13-5150 The brand name of the device is CaviWipes1 Extra Large, a surface disinfectant. The device has been assigned the product code LRJ (General Purpose Disinfectant) by the FDA and is classified as a Class I Medical Device. CaviWipes1 Extra Large is intended to be used to disinfect surfaces.