Starling SV CMM-ST5Recalls & reported problems
Cheetah Medical (Israel) Ltd · A portable, non-invasive cardiac output (CO) monitoring device. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Sep 2, 2022Class IIIOpen, Classified
Labeling has incorrect or incomplete Unique Device Identification (UDI) information; and the barcodes are not compliant with GS-1 standards.
Z-1817-2022 · Root cause: Process control · Recall details · FDA record ↗
Other Plethysmograph, Impedance devices
- uCor Heart Failure and Arrhythmia Management System SensorZoll Manufacturing Corporation · Plethysmograph, Impedance1,125 reports
- ZOLL PatchZoll Manufacturing Corporation · Plethysmograph, Impedance213 reports
- Starling CMMST5Cheetah Medical (Israel) Ltd · Plethysmograph, Impedance1 recall0 reports
- EV1000 PC2KEdwards Lifesciences LLC · PLETHYSMOGRAPH, IMPEDANCE10 reports
- CLEARSIGHT CSCSEdwards Lifesciences LLC · PLETHYSMOGRAPH, IMPEDANCE1 report
- EmpowerCTA®+ Injector System 017285Bracco Injeneering SA · Plethysmograph, Impedance1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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