SynchroWave Antenna Kit SW-1420Recalls & reported problems
Varian Medical Systems, Inc. · 20cm Long Tip Antenna and Cooling Circuit · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810563020540), received between Oct 15, 2019 and Oct 15, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
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.
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Cardiopulmonary Arrest1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 15, 2019Insufficient Device Problem Information; Insufficient Device Problem Information
(B)(6) CLINICAL EDUCATION SPECIALIST REPORTED THAT UPON ARRIVAL AT THE HOSPITAL, MTX GENERATOR WAS SAFETY CHECKED BY BIOMED. PATIENT WAS PLACED ON CT SCANNER AND ANESTHESIA WAS ADMINISTERED. INITIAL CT SCANS WERE OBTAINED AND MTX PROBE WAS PLACED. 45 SECONDS INTO THE BURN, PATIENT WENT INTO ASYSTOLE. CRNA AND ANESTHESIA MD ASSESSED, GAVE APPROPRIATE MEDS AND STABILIZED THE PATIENT. PROCEDURE CONTINUED AS NORMAL.
Patient problems: Cardiopulmonary Arrest
MAUDE report 9191488 ↗
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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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- 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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