CARESCAPE V100Recalls & reported problems
Ge Medical Systems Information Technologies, Inc. · V100 GENERIC ATO MODEL · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00840682103091), received between Jun 10, 2024 and Jun 10, 2024 — classified as 1 malfunction.
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Patient problems
- Tachycardia1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 10, 2024
PATIENT WITH SUSTAINED VENTRICULAR TACHYCARDIA (VTACH) TO 160S FOR APPROXIMATELY 2 MINUTES. GE TELEMETRY READING MEDIUM LEVEL YELLOW ALARM AND READING RHYTHM AT TACHY. REGISTERED NURSE WAS AT BEDSIDE PROVIDING PATIENT CARE. RAPID RESPONSE CALLED WHEN VTACH EVENT BEGAN.
Patient problems: Tachycardia
MAUDE report 19497574 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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