Z-1402-2017 Class II Terminated

Recalled by Metrex Research, LLC. — Romulus, MI

Recall Details

Product Type
Devices
Report Date
March 15, 2017
Initiation Date
January 20, 2017
Termination Date
September 1, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
960 cases

Product Description

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.

Reason for Recall

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

Distribution Pattern

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

Code Information

Lot No. 16-2340PA