Metrex Research, LLC.: Medical Device Recall in 2017 - (Recall #: Z-1402-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: January 20, 2017

Date Posted: March 15, 2017

Recall Number: Z-1402-2017

Event ID: 76318

Reason for Recall:

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

Status: Terminated

Product Quantity: 960 cases

Code Information:

Lot No. 16-2340PA

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated