Cook Spectrum G49802Recalls & reported problems
Cook Incorporated · Spectrum, Central Venous Tray Minocycline/Rifampin Impregnated Triple Lumen Polyurethane Catheter · Class 2
All models of Cook Spectrum (67)
Data updated Oct 16, 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 00827002498020), received between May 31, 2016 and May 31, 2016 — classified as 1 injury.
The most frequently reported specific device problem is “Migration or Expulsion of Device” (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
- Migration or Expulsion of Device1
Patient problems
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 31, 2016Migration or Expulsion of Device; Migration or Expulsion of Device
(B)(4): NEW CENTRAL VENOUS LINE CONFIRMED BY X-RAY AS LOCATED IN SUPERIOR VENA CAVA (VEIN). THE (B)(6) YEAR OLD PATIENT WITH ALTERED MENTAL STATUS APPROXIMATELY 4 DAYS LATER LEADING TO ACTIVATION OF CODE STROKE. CAT SCAN REVEALS CATHETER IS ACTUALLY IN THE INNOMINATE ARTERY AND PATIENT SUFFERED WATERSHED STROKE IN THE ANTERIOR CEREBRAL ARTERY (ACA) & MIDDLE CEREBRAL ARTERY (MCA) TERRITORY. LINE REMOVED IMMEDIATELY. ADDITIONAL INFORMATION RECEIVED ON 09 MAY 2016: THE PATIENT IS REPORTED TO HAVE BEEN IN REHABILITATION.
Patient problems: No Code Available
MAUDE report 5688079 ↗
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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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