PMT CORPORATION - STEREOTACTIC 2103-19-30Recalls & reported problems
Pmt Corporation · DEPTHALON ANCHOR BOLT, FOR 3.2MM DRILL, FOR VISUALASE 1.65MM PROBE · 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 00650551039051), received between Mar 31, 2025 and Mar 31, 2025 — classified as 1 malfunction.
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Insufficient Device Problem Information1
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.
MalfunctionMar 31, 2025Insufficient Device Problem Information; Appropriate Device Problem Term/Code Not Available; Insufficient Device Problem Information; Appropriate Device Problem Term/Code Not Available
REPORTED PROBLEM: (2) 30MM BOLTS BROKE IN THE SKULL AND THE DOCTOR ENDED UP ABANDONING THE SITES AND HAD TO DIG THEM OUT. I WAS TOLD DR. (B)(6) HAD TO RE-DRILL MULTIPLE TIMES AT THE SAME SITE BECAUSE HE WAS HAVING TROUBLE ACCURATELY PLACING THE ANCHOR BOLT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21732986 ↗
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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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