Geiger TCU Reusable Electrode 201-DRecalls & reported problems
Dermatologic Lab And Supply, Inc. · CAUTERY TIP, GEIGER D TIP, BALL, 1in SHAFT, EACH. Medical Device. · Class 2
Data updated Oct 18, 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 00609960000893), received between Dec 16, 2021 and Dec 16, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Activation Failure” (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
- Activation Failure1
- Positioning Failure1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 16, 2021Positioning Failure; Activation Failure; Positioning Failure; Activation Failure
THE HEALTHCARE PROFESSIONAL REPORTED THAT DURING A PULSERIDER-ASSISTED COIL EMBOLIZATION OF A RUPTURED ANTERIOR COMMUNICATING ARTERY (ACOM) ANEURYSM, AN APPROACH WAS MADE FROM THE RIGHT FEMORAL ARTERY WITH A 9F SHEATH. A 9F OPTIMO¿ BALLOON GUIDE CATHETER (TOKAI MEDICAL) WAS ADVANCED TOWARD THE LEFT INTERNAL CAROTID ARTERY (ICA). FROM THERE, A SOFIA¿ 6F INTERMEDIATE CATHETER (MICROVENTION) WAS ADVANCED TO THE LEFT ANTERIOR CEREBRAL ARTERY (ACA)-A1 SEGMENT. FROM THIS ROUTE, A PROWLER SELECT PLUS MICROCATHETER WAS ADVANCED TO THE FRONT OF THE ANEURYSM ON THE ACOM, AND THE COMPLAINT PRODUCT, A PULSERIDER T 3MM, 8MM ARCH ANEURYSM NECK RECONSTRUCTION DEVICE (ANRD) (201D / 3060357804) WAS INSERTED FOR IMPLANT. THE PULSERIDER ANDR WAS ADVANCED, BUT THE DIRECTION OF THE LEAFLET DID NOT FIT. AFTER CHANGING THE DIRECTION ABOUT FIVE TIMES, THE DEVICE WAS DEPLOYED AS INTENDED AND THE PULSERIDER WAS IMPLANTED. THE PROWLER SELECT PLUS MICROCATHETER WAS LOWERED TO THE DETACH POINT, BUT THE MARKER OF THE LEG DID NOT OPEN WELL (ONLY ABOUT HALF OF THE BLOOD VESSEL OPENED), AND THERE IS A POSSIBILITY THAT THE DELIVERY WIRE WAS ENTANGLED AND NOT BEING ABLE TO DETACH. THEREFORE, THE MICROCATHETER WAS RE
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13019539 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page