FDA Device recall Z-0110-2015
Mortara Surveyor S12 and Surveyor S19 Patient Monitors
- FDA Device
- Class II
- terminated
- Published 2014-10-29
On 2014-10-29 the FDA classified a Class II recall of Mortara Surveyor S12 and Surveyor S19 Patient Monitors by Mortara Instrument, citing 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 mou….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0110-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-10-07 |
| Published | 2014-10-29 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Mortara Instrument |
| Distribution | US |
Product
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 analysis, 12-Lead resting ECG, Cardiac output (C)). The Mortara Surveyor Patient Monitor is a prescription device intended to be used by healthcare professionals in all areas of a healthcare facility.
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
Identifiers
| code_info | Unit Serial Number 113400177138 113400177139 114260218985 114260218986 114260218987 114360228306 114330225509 1…Unit Serial Number 113400177138 113400177139 114260218985 114260218986 114260218987 114360228306 114330225509 114330225510 114330225511 114330225512 114330225513 114330225514 114330225515 114330225516 113430180113 114100196465 114040191976 114090196324 113490185858 113490185860 112090110348 113030149744 113030149745 113460182773 113460182774 113460182775 113460182776 113460182777 113460182778 113460182779 113460182780 113460182781 113460182782 113460182783 113460182784 113460182785 113460182786 113470184344 112090110349 112090110359 112090110360 112100110533 112100110538 112480143971 112480143973 112480143974 112490144251 112490144252 112490144253 112490144254 112490144255 113030149224 113030149746 113030149747 113030149748 113030149749 113030149750 113110157148 113110157149 113230166552 113230166553 113230166554 113230166555 113230166556 113230166557 113280169582 113300171794 113300171795 113450181352 113450181353 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0110-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.