Medrad Mr Inc: Medical Device Recall in 2014 - (Recall #: Z-0810-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Medrad Veris MR Monitor units The system is intended to monitor physiological parameters of patients within any healthcare environment. The user, responsible to interpret the monitored data made available, will be a professional healthcare provider. Physiological data, gas monitoring, system alarms, and patient analysis will be available to the care provider from the monitor.

Product Classification:

Class II

Date Initiated: November 21, 2013

Date Posted: January 29, 2014

Recall Number: Z-0810-2014

Event ID: 66996

Reason for Recall:

The main board, P/N 301641, installed in some Medrad Veris MR Monitor units may be faulty and could lead to unexpected shutdown of the system while in use, resulting in the loss of vital signs information from the monitor.

Status: Terminated

Product Quantity: 922 units

Code Information:

P/N 301641, Catalog #s 3011992, 3011992W, 3011993, 3011993W, 3011994, 3011994W, 3011996, 3011996W, 3014268, 3014268W, with multiple serial numbers.

Distribution Pattern:

Worldwide Distribution: US (nationwide) and Internationally to: Canada.

Voluntary or Mandated:

Voluntary: Firm initiated