FDAFebruary 15, 2018device

Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Some boxes are labeled as Visistat Wide devices, when in fact the contain Visistat Regular devices. The 6 individually packaged units within the boxes are correctly labeled.

What to do

FDA enforcement status: Terminated

Brands named

teleflex medicalteleflex

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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