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Teleflex Medical recalls Weck, Electrosurgical Coagulation Suction Tube 8 (20.0cm), 11 French, with Stylet, Teleflex Medical, Research Triangle,
Recalled January 22, 2014 · FDA recall Z-0771-2014 · Teleflex Medical
Hazard
Sterility cannot be guaranteed. · FDA Class II
Units
17,450 ea
Sold at
Nationwide Distribution.
Description
Sterility cannot be guaranteed.
Product
Weck, Electrosurgical Coagulation Suction Tube 8 (20.0cm), 11 French, with Stylet, Teleflex Medical, Research Triangle, NC 27709. Intended to remove tissue and control bleeding by use of high-frequency electrical current.
Manufacturer(s)
Teleflex Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →