N/A 24094Recalls & reported problems
Medtronic Ps Medical, Inc. · CATH 24094 VENT STD INCL SNAP BASE · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00763000030889), received between May 28, 2025 and May 28, 2025 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Disconnection” (2 reports).
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Disconnection2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 28, 2025Disconnection; Disconnection
MEDTRONIC RECEIVED INFORMATION REGARDING AN ADJUSTABLE SHUNT. IT WAS REPORTED THAT THE SNAP SHUNT ASSEMBLY WAS COMING UN-SNAPPED AFTER IMPLANTATION. THE PATIENT RETURNED TO SURGERY ON (B)(6) 2025 FOR REMOVAL OF THE SNAP, AND A NEW SHUNT WAS IMPLANTED WITH A NON SNAP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22100581 ↗MalfunctionMay 28, 2025Disconnection; Disconnection
MEDTRONIC RECEIVED INFORMATION REGARDING AN ADJUSTABLE SHUNT. IT WAS REPORTED THAT THE SNAP SHUNT ASSEMBLY WAS COMING UN-SNAPPED AFTER IMPLANTATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22100461 ↗
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- Strata® 42866Medtronic Ps Medical, Inc. · Shunt, central nervous system and components1 death160 reports
- proGAV 2.0® FX410TChristoph Miethke GmbH & Co. KG · Shunt, central nervous system and components119 reports
- Becker® 46128Medtronic Ps Medical, Inc. · Shunt, central nervous system and components1 recall50 reports
- PROGAV 2.0 FX643TAesculap AG · Shunt, central nervous system and components100 reports
- proSA® FV701TChristoph Miethke GmbH & Co. KG · Shunt, central nervous system and components82 reports
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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