AI system
- System
-
Samsung Galaxy Fit heart-rate monitor and Galaxy Watch ECG app
- Model
-
Not assessed
- Release
-
Exact release not established.
- Application developer
-
Samsung Electronics - Role
-
The wearable recorded the rapid heart-rate episode for later clinical assessment.
- Configuration
-
The initial event involved a Galaxy Fit SM-R370. A later report involved a Galaxy Watch Series 4.
- Inputs and outputs
-
Not assessed
- Autonomy
-
Not assessed
- Workflow
-
The wearer uses a Samsung Galaxy band or watch with heart-rate tracking or the ECG app. A symptomatic arrhythmia occurs while the device is worn and the reading or trace is shown to a clinician. A clinician confirms the rhythm and treats it.
- Human oversight
-
Not assessed
- Relation to AI
-
The band's heart-rate algorithm recorded the 188 bpm episode that documented the tachycardia. Clinicians diagnosed WPW on a 12-lead ECG and performed the ablation. The echo relied on the Galaxy Watch ECG app's trace, read by cardiologists.
- AI contribution
-
The band's heart-rate algorithm recorded the 188 bpm episode that documented the tachycardia. Clinicians diagnosed WPW on a 12-lead ECG and performed the ablation. The echo relied on the Galaxy Watch ECG app's trace, read by cardiologists.
Benefits
- Outcome identifiers
-
Not assessed
- Benefit
-
recorded a peak resting pulse rate of 188 beats per minute
- Category
-
Improved Physical Health
- Status
-
Not assessed
- Beneficiary groups
-
People.
- Beneficiaries
-
Not assessed
- Reach
-
Not assessed
- Distribution and access
-
Not assessed
- Duration
-
Not assessed
- Expected?
-
Yes
- Costs and harms
-
Not assessed
Measurement
- Studies
-
Not assessed
- Study design
-
Not assessed
- Measurement
-
Not assessed
- Setting and sample
-
Not assessed
- Measures
-
recorded a peak resting pulse rate of 188 beats per minute
- Comparison
-
Not assessed
- Results
-
recorded a peak resting pulse rate of 188 beats per minute
- Additional value from AI
-
Not assessed
- Limitations
-
Not assessed
- Denominators
-
Not assessed
- Materials for replication
-
Not assessed
Money
- Kind of value
-
Not assessed
- Amount
-
Not assessed
- Currency and prices
-
Not assessed
- Period and unit
-
Not assessed
- Realization
-
Not assessed
- Recipients and payers
-
Not assessed
- Gross or net
-
Not assessed
- Included costs
-
Not assessed
- Comparison
-
Not assessed
- Method
-
Not assessed
- Return and payback
-
Not assessed
People and places
- Participants
-
Developer:
Samsung Electronics. - Jurisdictions
-
Developer:
South Korea. - Ownership and control
-
Not assessed
- Dependencies
-
Not assessed
- Cross-border connections
-
Not assessed
- Geopolitical implications
-
Not assessed
Follow-up
- Conditions for replication
-
The device recording is reviewed promptly. A 12-lead ECG or inpatient monitoring is available for confirmation. Definitive therapy (ablation, drugs, device) is accessible.
- Replication attempts
-
1 follow-up entries. Benefit recurred: 1.
- Later findings
-
24 March 2021. After catheter ablation on 29 June 2020 the patient kept using a smartwatch to monitor for recurrence, as the case report published in March 2021 records.
- Availability
-
Not assessed
- Institutional decision
-
Not assessed
- Grounds
-
Not assessed
- Action and result
-
Not assessed
- Success criterion
-
Not assessed
Evidence
- Source numbers
-
AIBD-0024-source-0001–0003
- Citations
-
Numbered references below.
- Language
-
Not assessed
- Source relationships
-
Independent
- Original evidence
-
Not assessed
- Access and versions
-
Not assessed
- Supported findings
-
Not assessed
- Evidence links
-
Not assessed
- Evidence strength
-
Not assessed
- Missing evidence
-
Not assessed
Grades
- Assessed benefits
-
People.
- Depth
-
People: 2.
- Reasons
-
People: A young worker's band documented a 188 bpm tachycardia. With a routine ECG showing WPW the next day and her symptoms, it backed referral for electrophysiology study. Successful radiofrequency catheter ablation came 11 days after the recorded episode. A material benefit to one person, though the diagnosis itself came from the routine ECG.
- Observed or intended
-
Not assessed
- Rubric
-
Not assessed
- Assessor and date
-
Not assessed
- Alternative assessments
-
Not assessed
- Fill
-
Independently studied
Entry details
- Kind
-
Not assessed
- Related entries
-
No Samsung wearable incident exists; the nearest wearable false alarm is Apple Watch Crash Detection misclassifying skiing and dialing 911, harming watch users and dispatchers, the inverse of a Galaxy Fit's true 188 bpm detection.
Apple Devices Mistook Skiing Activities, Dialed False Distress Emergency Calls
- Field
-
Healthcare (cardiology; occupational medicine). Consumer wearables.
- Purpose
-
The Galaxy Fit's optical sensor is built to track heart rate, and the Galaxy Watch ECG app to record single-lead ECGs for rhythm assessment. The benefit came from those functions.
- Dates
-
Date basis unassessed: 2020 (precision unassessed). Updated: 22 October 2026.
- Stage
-
Not assessed
- Version
-
SHA-256: 67a92f155e7f…
References
- Other identifiers
-
AI Incident Database: 463.
- Category mappings
-
Not assessed
- Brief
-
Not assessed
- Revisions
-
8 revisions. Latest: 22 October 2026.
Sources
-
Peer-reviewed study Independent author
Bogár B et al. (2024). Detection of Arrhythmias Using Smartwatches—A Systematic Literature Review. Healthcare 12(9):892.
Samsung Galaxy Fit was used for arrhythmia registration in one patient.
-
Case report Independent author
Mun E, Hong J, Kwon S, Lee SH, Kim W, Lee C (2021). Digital health care and arrhythmia: a case of WPW syndrome in South Korea, 2020. Annals of Occupational and Environmental Medicine 33:e8. (Authors at Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine; hospital staff, not Samsung Electronics.)
her peak resting pulse rate reached 188 beats per minute
-
Case report Independent author
Avidan Y, Tabachnikov V, Danon A, Schliamser JE (2024). Polymorphic Ventricular Tachycardia Detected by a Smartwatch in a Patient With Recurrent Syncope. JACC: Case Reports.
After 1 year of outpatient follow-up, there were no further clinical events.