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Cook Spectrum G36209Recalls & reported problems

Cook Incorporated · Cook Spectrum PICC Set Minocycline/Rifampin Impregnated Single Lumen Silicone · Class 2 · Implant

All models of Cook Spectrum (67)

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 00827002362093), received between Sep 20, 2017 and Sep 20, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Entrapment 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 18, 2026.

Most reported problems

Device problems

  • Entrapment of Device1
  • Split1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 20, 2017Entrapment of Device; Split

    THE CUSTOMER REPORTED THAT THE WIRE STARTED TO SPLIT AND WAS STUCK TO THE INSIDE OF THE CATHETER. THERE WERE NO INJURIES OR ADDITIONAL MEDICAL INTERVENTION REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6878998 ↗

Other Catheter,intravascular,therapeutic,long-term greater than 30 days devices

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Sources and updates

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