Cook Spectrum G43982Recalls & reported problems
Cook Incorporated · Spectrum, Central Venous Catheter Tray Minocycline/Rifampin Antibiotic Impregnated Double Lumen Polyurethane · Class 2
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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00827002439825), received between Aug 7, 2019 and Aug 7, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Crack” (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
- Crack1
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.
InjuryAug 7, 2019Crack; Crack
ADDITIONAL INFORMATION WAS RECEIVED ON 25SEP2019 STATING THAT THE FITTING WAS NOT CONNECTED TO ANYTHING AND IS NOT AVAILABLE FOR RETURN. THE CUSTOMER IS UNABLE TO PROVIDE THE LENGTH OF TIME THE DEVICE WAS IN PLACE. THERE WAS NO FORCE EXERTED ON THE CATHETER.
Patient problems: No Code Available
MAUDE report 8871650 ↗
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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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