Epix® Electrosurgical Probe C7302Recalls & reported problems
Applied Medical Resources Corporation · Reusable L-Hook Probe with Male Post. · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00607915127640), received between Apr 29, 2016 and Jul 7, 2017 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (2 reports).
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
- Break2
Patient problems
- No Consequences Or Impact To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 7, 2017Break; Break
PROCEDURE PERFORMED: "LC". PATIENT STATUS: "FINE". "THIS INSTRUMENT WAS FIRST USED. IN SURGERY, THE L-HOOK TIP FELL OFF AND SURGEON HAS BEEN REMOVED IT FROM PATIENT BODY." TYPE OF INTERVENTION: "REMOVED IT FROM PATIENT BODY."
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6695622 ↗MalfunctionApr 29, 2016Break; Break
NEPHRECTOMY - "THE THREAD OF PROBE CONNECTOR IS BROKEN IN SURGERY SUDDENLY. PLEASE CONSULT WITH ATTACHED PHOTO." PATIENT STATUS - "FINE".
Patient problems: No Consequences Or Impact To Patient
MAUDE report 5620073 ↗
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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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