NA 44102Recalls & reported problems
Medtronic Ps Medical, Inc. · RES 44102 VENT CATH 18MM SIDE IN IMP · Class 2 · Implant
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 00643169466777), received between Apr 28, 2017 and Apr 28, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Leak/Splash” (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.
Most reported problems
Device problems
- Leak/Splash1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 28, 2017Leak/Splash; Leak/Splash
IT WAS REPORTED TO MEDTRONIC NEUROSURGERY THAT DURING PRE-OPERATIVE PREPARATION, THE DEVICE WAS PRIMED, BUT WATER LEAKED FROM THE RESERVOIR. ACCORDING TO THE REPORT, SINCE A DEVICE MALFUNCTION OCCURRED, THE DEVICE WAS NEVER IMPLANTED AND WAS DISCARDED IN THE HOSPITAL.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6531871 ↗
Other PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR devices
- N/A 44010Medtronic Ps Medical, Inc. · Port & catheter, implanted, subcutaneous, intraventricular30 reports
- NA 44010Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR9 reports
- NA 41406Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR2 reports
- N/A 41406Medtronic Ps Medical, Inc. · Port & catheter, implanted, subcutaneous, intraventricular2 reports
- NA 41407Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR2 reports
- NA 27051Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR1 report
- Innervision 27065 BMedtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR1 report
- N/A 41409Medtronic Ps Medical, Inc. · Port & catheter, implanted, subcutaneous, intraventricular1 report
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.
How reports and recalls are matched · Editorial policy · Report an error on this page