CODMAN® VPV® 823192RRecalls & reported problems
Integra Lifesciences Production Corporation · CODMAN® VPV System · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10381780538325), received between Jan 7, 2025 and Jan 11, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Output 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.
Reports received per month
Most reported problems
Device problems
- Output Problem1
- Overheating of Device1
- Smoking1
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.
MalfunctionJan 11, 2025Overheating of Device; Output Problem; Overheating of Device; Output Problem
IT WAS REPORTED THAT THE CODMAN VPV PROGRAMMER REVISED (823192R) INCURRED AN "ERROR: FAILURE TO SET PROGRAMMING AND OVERHEAT". IT UNKNOWN UNDER WHAT CIRCUMSTANCE THIS EVENT OCCURRED. NO PATIENT INJURY OR SURGICAL DELAY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21133286 ↗MalfunctionJan 7, 2025Smoking; Smoking
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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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