Mortara Surveyor S12 and Surveyor S19 Patient Monitors — Class II medical device recall Z-0110-2015
Terminated recall by Mortara Instrument, Inc, reported 2014-10-29, distributed nationwide. Martara Instrument, Inc. has recently became aware of a potential safety hazard involving our Surveyor rand S1
| Recall number | Z-0110-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mortara Instrument, Inc, Milwaukee, WI, United States |
| Recall initiated | 2014-10-07 |
| Classified | 2014-10-21 |
| Reported by FDA | 2014-10-29 |
| Terminated | 2015-02-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BD, CA, CL, DE, EG, GB, HR, IT, JO, LB, MA, MY, NL, OM, PH, PL, RO, SA, TH |
| Quantity | 624 |
| UPC / GTIN / UDI-DI | 00112220117311, 00112490144253, 00113030149745, 00113240166907, 00113240166914, 00113280169678, 00113370175190, 00113370175206, 00113370175213, 00113370175220, 00113410178150, 00113420179680, 00113430179786, 00113430179847, 00113430179854, 00113440180451, 00113450181585, 00113450181592, 00113460182770, 00113460182787, 00113470184290, 00113470184344, 00113470184368, 00113490185857, 00113490185864 and 37 more |
| Serial numbers | 112080109545, 112090110347, 112090110348, 112090110349, 112090110359, 112090110360, 112100110533, 112100110535, 112100110536, 112100110538, 112100110539, 112220117311, 112480143971, 112480143972, 112480143973, 112480143974, 112490144251, 112490144252, 112490144253, 112490144254, 112490144255, 113020148884, 113020149035, 113030149224, 113030149744 and 475 more |
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 for recall
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0110-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.