FDA Device recall Z-0927-2014
CARESCAPE Monitor B850, a multi-parameter high acuity patient monitor intended for use in multiple areas within a professional healthcare f…
- FDA Device
- Class II
- terminated
- Published 2014-02-12
On 2014-02-12 the FDA classified a Class II recall of CARESCAPE Monitor B850, a multi-parameter high acuity patient monitor intended for use in multiple areas within a professional healthcare f… by Ge Healthcare, citing there is a potential for communication loss associated with the F5-01 Frame when connected to CARESCAPE Patient Data Module (PDM) in the CARESCAPE Monitor B850. The PDM patient pa….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0927-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-12-20 |
| Published | 2014-02-12 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
CARESCAPE Monitor B850, a multi-parameter high acuity patient monitor intended for use in multiple areas within a professional healthcare facility. Product Usage: The CARESCAPE Monitor B850 is intended for use on adult, pediatric, and neonatal patients and on one patient at a time. The CARESCAPE Monitor B850 system is indicated for monitoring of Hemodynamic (including ECG, ST Segment, Arrhythmia Detection, ECG Diagnostic Analysis and Measurement, Invasive Pressure, Noninvasive Blood Pressure, Pulse Oximetry, Cardiac Output, Temperature, Impedance Respiration and SvO2 (Mixed Venous Oxygen Saturation)), Airway Gases (Fi/Et C02, 02, N20 and Anesthetic Agent), Spirometry, Gas Exchange (02 Consumption (VO2), C02 production (VCO2), energy expenditure (BE), and respiratory quotient (RQ)) and neurophysiological (including electroencephalography (EEG), Entropy, Bispectral Index (BIS) and Neuromuscular Transmission (NMT) Monitoring) status. The CARESCAPE Monitor B850 provides alarms, trends, snapshots and events, and calculations and can be connected to displays, printers and recording devices. The CARESCAPE Monitor B850 can be a stand-alone monitor or interfaced to other devices. It can also be connected to other monitors for bed to bed viewing and to data management software devices via a network. The CARESCAPE Monitor B850 is intended for use under the direct supervision of a licensed healthcare practitioner, or by personnel trained in proper use of the equipment in a professional healthcare facility. In addition to the healthcare practitioner, the CARESCAPE Monitor B850 is designed to provide configuration and troubleshooting capabilities to qualified service personnel.
Reason
There is a potential for communication loss associated with the F5-01 Frame when connected to CARESCAPE Patient Data Module (PDM) in the CARESCAPE Monitor B850. The PDM patient parameter acquisition module can sometimes spontaneously lose the communication with the host patient monitor when attached to the F5-01 Frame due to an issue with the PDM Ethernet communication hardware. The communicatio
Identifiers
| code_info | serial numbers: SEG09270517HX, SEG09270549HX, SEG09270551HX, SEG09270553HX, SEG09270554HX, SEG09270557HX, SEG09270559H…serial numbers: SEG09270517HX, SEG09270549HX, SEG09270551HX, SEG09270553HX, SEG09270554HX, SEG09270557HX, SEG09270559HX, SEG09270561HX, SEG09270562HX, SEG09270563HX, SEG09270564HX, SEG09270565HX, SEG09270566HX, SEG09270567HX, SEG09270568HX, SEG09270569HX, SEG09270583HX, SEG09270584HX, SEG09270585HX, SEG09270587HX, SEG09270588HX, SEG09270589HX, SEG09270591HX, SEG09270592HX, SEG09280596HX, SEG09280597HX, SEG09280598HX, SEG09280599HX, SEG09280600HX, SEG09280601HX, SEG09280602HX, SEG09280603HX, SEG09280604HX, SEG09280605HX, SEG09280606HX, SEG09280607HX, SEG09280608HX, SEG09280609HX, SEG09280610HX, SEG09280611HX, SEG09280612HX, SEG09280613HX, SEG09280614HX, SEG09280615HX, SEG09280616HX, SEG09280617HX, SEG09280618HX, SEG09280619HX, SEG09280620HX, SEG09280621HX, SEG09280622HX, SEG09280623HX, SEG09280624HX, SEG09280625HX, SEG09310656HX, SEG09310657HX, SEG09310658HX, SEG09310659HX, SEG09310660HX, SEG09310661HX, SEG09310662HX, SEG09310663HX, SEG09310664HX, SEG09310665HX, SEG09310666HX, SEG09310 |
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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-0927-2014%22
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