Recall Z-0110-2015 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Mortara Instrument, Inc
Mortara Surveyor S12 and Surveyor S19 Patient Monitors. Product Usage: They are indicated for use in adult & pediatric patient populations. They facilitate the monitoring of: Non-invasive blood pressure (NIBP), Impedance respiration, Invasive blood pressure (P1-P4), Temperature, Functional arterial oxygen saturation (SpO2), End-tidal & inspired CO2, ECG monitoring with arrhythmia and ST-segment a
| Date | Oct 22, 2014 (initiated Oct 7, 2014) |
| Status | Terminated |
| Reason | Martara Instrument, Inc. has recently became aware of a potential safety hazard involving our Surveyor rand S12 S19 Patient Monitors. A hazardous situation may be created when mounting these monitors using the 75mm VESA mounting hole pattern provided in the battery cover of these monitors. If the mounting screws provided by Mortara are not used and if the mounting screws used are longer than the p |
| Root cause | Device Design |
| Action | Mortar Instruments, Inc. sent an "Urgent Medical Device Correction" letter dated October 3, 2014. The letter was addressed to Health Care Administrator / Risk Manger and Director of Biomedical / Clinical Engineering.The letter described the problem and the product involved in the recall. Customers were advised to contact Mortara Technical Support at 1-888-667-8272 or TechSupport @mortara.com to schedule a service representative to update their Surveyor S12 and Surveyor S19 units or for additional questions they can contact their local Service Representative. The update will include replacemen |
| Quantity | 624 |
| Distribution | Worldwide Distribution: US (Nationwide) in the states of: AZ, AR, CA, DC, FL, ID, IL IN, KY, LA, ME, MD, MA, MI, MN, MO, MT, NV, NJ, NY, NC, OK PA, SC, TN, TX, VA, and WI; and internationally to: AUSTRALIA, BANGLADESH, CANADA, CHILE, CROATIA, EGYPT, GERMANY, ITALY, JORDAN, LEBANON, MALAYSIA, MOROCC |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K123556 | MORTARA SURVEYOR PATIENT MONITOR Mortara Instrument, Inc., Mar 22, 2013 |