Sophysa SM8ARecalls & reported problems
Sophysa · SOPHY MINI PROG.VALVE/8.PRESS. ANTICHAMBER · Class 2 · Implant
Data updated Oct 16, 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 03760124131215), received between Nov 25, 2016 and Nov 25, 2016 — classified as 1 malfunction.
The most frequently reported specific device problem is “Pressure 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 16, 2026.
Most reported problems
Device problems
- Pressure Problem1
Patient problems
- Hydrocephalus1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 25, 2016Pressure Problem; Pressure Problem
THE USER REPORTED A SUSPICION OF HYPODRAINAGE DUE TO A FAILURE OF THE VALVE (TESTED INTRAOPERATIVELY).
Patient problems: Hydrocephalus
MAUDE report 6127168 ↗
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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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