Kangaroo 711253CNRecalls & reported problems
Cardinal Health, Inc. · CO2 Detector with Bellows,Nasogastric Feeding Tube and Stylet · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10884521146136), received between May 27, 2020 and Sep 24, 2021 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (5 reports).
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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Detachment of Device or Device Component5
Patient problems
- Needle Stick/Puncture2
- Injury1
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
- Pain1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2021Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT WHEN GOING TO TAKE OFF THE STYLET, THE STYLET TIP FALLS OFF. THE NURSE WAS PUNCTURED AND BLED. THE NURSE REPORTED IT TO EMPLOYEE HEALTH. NO ACTIONS NEEDED AS THE PATIENT DID NOT HAVE AN ACTIVE GI BLEED THEREFORE IT WAS NOT CONSIDERED AN EXPOSURE. NO TREATMENT NEEDED.
Patient problems: Needle Stick/Puncture
MAUDE report 12530510 ↗MalfunctionAug 23, 2021Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT THE BLUE TIP STYLET SNAPPED OFF OF THE 12 FR DOBBHOFF FEEDING TUBE. NO PATIENT INJURY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12356977 ↗MalfunctionJun 5, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT THE DEVICE CAP BROKE OFF DURING REMOVAL OF STYLET.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10125906 ↗MalfunctionJun 3, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT WHILE REMOVING THE GUIDE WIRE AFTER FLUSHING, THE END CAP (STYLET) BROKE OFF EXPOSING THE WIRE AND THE WIRE PUNCTURED THE NURSE'S THUMB. THE NURSE CONTINUE TO EXPERIENCE SOME SORENESS. THE NURSE WENT TO THE OCCUPATIONAL AID STATION AND RECEIVED AN ANTIBIOTIC CREAM AND APPLIED BAND AID. THE NURSE IS DOING FINE.
Patient problems: Injury; Pain
MAUDE report 10116352 ↗MalfunctionMay 27, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT THE NURSE WAS REMOVING THE STYLET FROM A DOBBHOFF FEEDING TUBE AND THE CAP BROKE OFF EXPOSING THE WIRE AND CUT HER FINGER.
Patient problems: Needle Stick/Puncture
MAUDE report 10093703 ↗
Other TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices
- Bard® DigniShield® Stool Management System SMS002C. R. Bard, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)2 deaths525 reports
- CORTRAK* 2 ENTERAL ACCESS SYSTEM 20-0950Avanos Medical, Inc. · Tubes, gastrointestinal (and accessories)1 recall22 deaths134 reports
- Bard Tri-Funnel Replacement Gastrostomy Tube 000720Bard Access Systems, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 death170 reports
- EndoVive Safety PEG Kit M00566470Boston Scientific Corporation · TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 recall1 death111 reports
- Kangaroo 8884711253Cardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)152 reports
- Kangaroo 8884711253ECardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)100 reports
- NutraGlide Nasal Feeding Tube ENFT-05055-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- NutraGlide Nasal Feeding Tube ENFT-06090-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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