Perineologic 1Recalls & reported problems
Corbin Clinical Resources, LLC · The Perineologic PrecisionPoint™ Transperineal Access System is a sterile, single use, disposable, needle guide consisting, of a Carriage and a Rail Clamp Assembly and Access Needle, that is intended for use with a cylindrical style trans-rectal ultrasound transducer (0.7” to .85” diameter BK #8658 or equivalent) associated with a BK ProFocus ultrasound system and a biopsy needle. The PrecisionPoint™ Transperineal Access System is designed to stabilize a Perineologic Access Needle on the anatomy as a means to properly guide the anatomical placement of a biopsy needle into the prostate or other soft tissues through the use of ultrasound-assisted guidance. · Class 2
Data updated Oct 13, 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 B371P10020), received between Dec 18, 2025 and Dec 18, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Premature Activation” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Premature Activation1
Patient problems
- Needle Stick/Puncture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 18, 2025Premature Activation; Premature Activation
IT WAS REPORTED THAT THERE WAS DIFFICULTY REMOVING THE TROCAR FROM THE SECOND TO BOTTOM APERTURE OF THE CARRIAGE. THE NURSE PULLED OUT THE TROCAR FROM THE CARRIAGE BUT INADVERTENTLY POKED HER MIDDLE FINGER WITH THE ACCESS NEEDLE. IT WAS NOTED THAT THE NURSE WASHED AND SANITIZED THE NEEDLE PUNCTURE AND PLACED A BAND-AID. A PRECAUTIONARY PATIENT BLOOD TEST WAS PERFORMED TO DETERMINE IF ANY FURTHER ACTION WAS REQUIRED.
Patient problems: Needle Stick/Puncture
MAUDE report 23843488 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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