NATUS LUMBAR EXTERNAL DRAINAGE CATHETHER NT821706Recalls & reported problems
Natus Medical Incorporated · NATUS LUMBAR EXTERNAL DRAINAGE CATHETHER · Class 2
Data updated Oct 18, 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 00382830050524), received between Apr 27, 2025 and Apr 27, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 27, 2025Break; Break
NT821706, EXTERNAL DRAINAGE, LUMBAR CATHETER - LUMBAR DRAIN CATHETER SHEARING OFF DURING PLACEMENT WITH AN UNANTICIPATED SURGICAL PROCEDURE TO REMOVE THE CATHETER REMNANTS. PATIENT NEEDED LUMBAR DRAIN PLACED FOR CSF LEAK. ACCESS NEEDLE INSUFFICIENT LENGTH FOR BODY HABITUS. CATHETER SHEAR DURING MANIPULATIONS. PARTIAL CATHETER PIECE AND WIRE REMOVED SUCCESSFULLY AFTER OPERATIVE PROCEDURE.
Patient problems: Foreign Body In Patient
MAUDE report 21915994 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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