Medistim Asa: Medical Device Recall in 2018 - (Recall #: Z-0719-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully plan and accomplish surgical interventions.

Product Classification:

Class II

Date Initiated: April 25, 2017

Date Posted: March 7, 2018

Recall Number: Z-0719-2018

Event ID: 78973

Reason for Recall:

A system component overheated causing melting of the connector and emission of smoke through the systems loudspeaker opening.

Status: Terminated

Product Quantity: 2

Code Information:

UDI: 7070554101198 Serial#: 1170 and 1294

Distribution Pattern:

Distributed to New York.

Voluntary or Mandated:

Voluntary: Firm initiated