RenalCryo™ RS-17LRecalls & reported problems
Varian Medical Systems, Inc. · Endocare™ 1.7 mm RenalCryo™ Long Shaft Cryoprobe · Class 2
Data updated Oct 16, 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 00810563020052), received between Apr 5, 2016 and Apr 5, 2016 — 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 16, 2026.
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Burn, Thermal1
- Skin Inflammation/ Irritation1
- Unspecified Tissue Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 5, 2016Insufficient Device Problem Information
DURING THE PROCEDURE THE PERC-17 PROBE GAVE THE PATIENT A DIME SIZED THERMAL INJURY TO THE SKIN.
Patient problems: Burn, Thermal; Skin Inflammation/ Irritation; Unspecified Tissue Injury
MAUDE report 5547522 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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