S-CATH™ Esophageal Temperature Probe CS-27ST (Straight)Recalls & reported problems
CIRCA Scientific, Inc. · 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 10860237000207), received between Jan 10, 2020 and Jan 10, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Migration or Expulsion of Device” (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
- Migration or Expulsion of Device1
Patient problems
- Perforation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 10, 2020Migration or Expulsion of Device
ESOPHAGEAL PERFORATION. PATIENT UNDERWENT SURGERY AND WAS TREATED WITH AN ESOPHAGEAL STENT. ESOPHAGUS HAD TWO HOLES, DESCRIBED BY PHYSICIAN AS BEING ABOUT 8F AS IF THE PROBE HAD GONE OUT OF THE ESOPHAGUS AND THEN BACK INTO THE ESOPHAGUS. CIRCA USED TO MONITOR TEMPERATURE DURING A CARDIAC ABLATION PROCEDURE ABOUT 2 WEEKS PRIOR. THERE WAS NO THERMAL INJURY TO THE ESOPHAGUS.
Patient problems: Perforation
MAUDE report 9578687 ↗
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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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