DEPTHALON® 2102-08-091Recalls & reported problems
Pmt Corporation · sEEG, PLATINUM, 8 CONTACT, MINI CONNECTOR, REMOVABLE STYLET, FOR 2.4MM DRILL · 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 00650551041634), received between Jan 31, 2024 and Jan 31, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Separation Problem” (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.
Reports received per month
Most reported problems
Device problems
- Separation Problem1
Patient problems
- Foreign Body In Patient1
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 31, 2024Separation Problem; Separation Problem
EMAIL RECEIVED FROM DOCTOR ON NOVEMBER 10, 2023. I WANT TO OPEN A "TICKET" FOR THE COMPANY TO REVIEW THE CASE WE HAD LAST WEEK WHERE THE ELECTRODE GOT TORN. THERE IS A TINY FRAGMENT (THE TIP) THAT IS STUCK IN THE MOTOR CORTEX SO I CANNOT PULL IT OUT. WE ARE STILL TRYING TO FIGURE OUT IF THE PATIENT CAN HAVE AN MRI (I BELIEVE HE CAN BUT WE ARE TRYING TO UNDERSTAND) AND ALSO WHAT CAN BE THE REASON. I TALKED TO SEVERAL FRIENDS THAT ARE QUITE EXPERIENCED WITH SEEG WORKING WITH PMT ELECTRODES AND NONE HAD THIS ISSUE. I MYSELF DID AT LEAST 50 CASES WITH PMT AND MORE THAN 500 ELECTRODES AND NEVER HAD THIS ISSUE.
Patient problems: Foreign Body In Patient; Insufficient Information
MAUDE report 18617662 ↗
Other Electrode, Depth devices
- Spencer Probe Depth Electrode SD04R-AP58X-000Ad-Tech Medical Instrument Corporation · ELECTRODE, DEPTH1 recall0 reports
- NA MICRODEEP DEPTH ELECTRODEDixi Medical · Electrode, Depth1 recall0 reports
- Spencer Probe Depth Electrode SD06R-AP58X-000Ad-Tech Medical Instrument Corporation · ELECTRODE, DEPTH1 recall0 reports
- NA MICRODEEP DEPTH ELECTRODEDixi Medical · Electrode, Depth1 recall0 reports
- NA MICRODEEP DEPTH ELECTRODEDixi Medical · Electrode, Depth1 recall0 reports
- NA MICRODEEP DEPTH ELECTRODEDixi Medical · Electrode, Depth1 recall0 reports
- NA MICRODEEP DEPTH ELECTRODEDixi Medical · Electrode, Depth1 recall0 reports
- NA MICRODEEP DEPTH ELECTRODEDixi Medical · Electrode, Depth1 recall0 reports
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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