Nico Corp.: Medical Device Recall in 2016 - (Recall #: Z-2045-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Myriad handpiece Tissue morcellator

Product Classification:

Class II

Date Initiated: February 24, 2014

Date Posted: June 29, 2016

Recall Number: Z-2045-2016

Event ID: 74191

Reason for Recall:

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.

Status: Terminated

Product Quantity: 63 units

Code Information:

13ga, 13cm Myriad Handpiece Part number: NN-8004 Lots 1444664 and 1508994

Distribution Pattern:

US Distribution to the states of : OR, IL, IA, NC, TX, CA, GA, OH, WI, AR, MI, MD, IN.

Voluntary or Mandated:

Voluntary: Firm initiated