Home / Recalls / Medical Devices
Nico Corp. recalls Myriad handpiece Tissue morcellator
Recalled June 29, 2016 · FDA recall Z-2045-2016 · Nico
Hazard
This recall has been initiated due to a defective component within the handpiece which will cause the handpiece to fail. The failure will result in the inability to cut tissue with the handpiece, rendering it non-functional. Should this failure occur, a replacement Myriad handpiece will be required. If a replacement handpiece is not available, alternate instrumentation for tissue removal will be necessary. · FDA Class II
Units
63 units
Sold at
US Distribution to the states of : OR, IL, IA, NC, TX, CA, GA, OH, WI, AR, MI, MD, IN.
Description
This recall has been initiated due to a defective component within the handpiece which will cause the handpiece to fail. The failure will result in the inability to cut tissue with the handpiece, rendering it non-functional. Should this failure occur, a replacement Myriad handpiece will be required. If a replacement handpiece is not available, alternate instrumentation for tissue removal will be necessary.
Product
Myriad handpiece Tissue morcellator
Manufacturer(s)
Nico Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →