FDAJanuary 20, 2017device
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...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Metrex is recalling the CaviWipes Extra Large because they may have been contaminated during the packaging process.
What to do
FDA enforcement status: Terminated
Brands named
metrex researchmetrex
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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