CODMAN HAKIM RICKHAM 82-3852Recalls & reported problems
Cerenovus, Inc. · CODMAN HAKIM Programmable Valve with Unitized Large RICKHAM Reservoir and Non-Unitized Distal Catheter 120cm Operating Pressure: 30mm H2O to 200mm H2O (294 Pa - 1960 Pa) programmable in steps of 10mm H2O (98 Pa) Includes: Ventricular Catheter 14cm, Stylet, Introducer and Information Manual · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886704041887), received between Feb 27, 2024 and Feb 27, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Device Difficult to Program or Calibrate” (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
- Device Difficult to Program or Calibrate1
Patient problems
- Headache1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 27, 2024Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate
A FACILITY REPORTED A HAKIM VALVE (ID 823852) WAS IMPLANTED ON (B)(6) 2012 VIA VENTRICULOPERITONEAL (VP) SHUNT. THE VALVE MALFUNCTIONED AND WAS NOT ABLE TO RESET SHUNT PRIOR TO SURGERY, THEREFORE IT WAS EXPLANTED AND REPLACED ON (B)(6) 2024 DUE TO INABILITY TO REPROGRAM. THE PATIENT EXPERIENCED POSITIONAL HEADACHES CONSISTENTLY WITH LOW PRESSURE AND IS RECOVERING WELL.
Patient problems: Headache
MAUDE report 18788692 ↗
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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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