Invivo Corporation: Medical Device Recall in 2016 - (Recall #: Z-2688-2016)

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:

Invivo Sentinelle Venguard Breast MRI Auxiliary Table/Tabletop with 8/16 Channel Coil Array for GE 1.5T/3T MRI Systems.

Product Classification:

Class II

Date Initiated: May 6, 2016

Date Posted: September 7, 2016

Recall Number: Z-2688-2016

Event ID: 74064

Reason for Recall:

A diode was inadvertently not assembled into the system, which may result in coil overheating

Status: Terminated

Product Quantity: 3

Code Information:

Model #: 9896-032-14382; Serial #: 13 (production order 301128446), 14 (production order 301153586), and 15 (production order 301153587).

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated