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Norav 1200 Series PC-ECG

NORAV MEDICAL LTD. · Model 1200HRT · UDI-DI 07290110252908

MWI Prescription
10
510(k) clearances
2,065
Adverse events (45 deaths)
85
Recalls
172
Facilities

Description

PC-ECG Acquisition Device for High Resolution Resting-ECG and Stress-Test ECG recordings with ECG Trigger Output and IEC type labelling.

Recalls

DateFirmReason
2026-08-21Midmark CorporationA performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
2026-08-21Midmark CorporationA performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
2026-08-21Midmark CorporationA performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
2026-08-21Midmark CorporationA performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
2026-07-20GE Medical Systems Information Technologies IncSoftware issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and
2026-07-20GE Medical Systems Information Technologies IncSoftware issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and
2026-07-20GE Medical Systems Information Technologies IncSoftware issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and
2026-07-20GE Medical Systems Information Technologies IncSoftware issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and
2026-07-10GE Medical Systems Information Technologies IncPortrait Core Services Software version V1.2.0 Security Vulnerability
2026-01-30Covidien LLCDue to complaints and investigations stating that alarms from the primary patient bedside monitor was not alarming/being transmitted and received on the remote patient monitoring s

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.