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Teleflex Medical recalls Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.
Recalled April 4, 2018 · FDA recall Z-1193-2018 · Teleflex Medical
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. · FDA Class II
Units
12 units
Sold at
KS
Description
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.
Product
Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.
Manufacturer(s)
Teleflex Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →