Kangaroo 8884752042ERecalls & reported problems
Cardinal Health, Inc. · Y-Port/PEG Adapter · Class 2
- 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 30884521664061), received between Oct 17, 2018 and Jan 23, 2023 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (2 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
- Fluid/Blood Leak2
- Leak/Splash2
- Crack1
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- No Known Impact Or Consequence To Patient1
- No Patient Involvement1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 23, 2023Fluid/Blood Leak; Detachment of Device or Device Component; Fluid/Blood Leak; Detachment of Device or Device Component
CUSTOMER REPORTS: THE YELLOW PIECE CAME OUT AND WILL NOT STAY IN. PER ADDITIONAL INFORMATION PROVIDED ON 1/23/23, THE PRODUCT APPEARS TO HAVE LEAKED AS IT DID NOT FIT SNUGGLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16225551 ↗MalfunctionFeb 22, 2022Crack; Crack
THE CUSTOMER REPORTED THE REPLACEMENT FITTING HAS CRACKED. AFTER BEING AT THE CLIENT, IT WOULD APPEAR THAT THE CAREGIVERS USE TWO FORCEPS TO OPEN THE CAP THAT IS USED TO CLOSE THE NUTRITION PORT. ADDITIONAL INFORMATION RECEIVED STATED THE DEVICE WAS LEAKING FORMULA DUE TO THE ISSUE. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13577505 ↗MalfunctionJun 4, 2021Fluid/Blood Leak; Fluid/Blood Leak
THE CUSTOMER REPORTED THE Y PORT ADAPTOR LEAKS AT THE POINT WHERE IT CONNECTS TO THE FUNNEL. NO PATIENT INJURY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11941866 ↗MalfunctionOct 24, 2018Leak/Splash; Leak/Splash
ACCORDING TO THE REPORTER, THE Y CONNECTOR IS CRACKED CAUSING A LEAKAGE AT THE Y-CONNECTOR ENFIT. THERE IS NO REPORTED PATIENT HARM AND NO ADDITIONAL DETAILS ARE AVAILABLE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7999757 ↗MalfunctionOct 17, 2018Leak/Splash; Leak/Splash
ACCORDING TO THE REPORTER, THE Y-CONNECTOR CONNECTION IS CRACKED CAUSING LEAKAGE. THERE IS NO REPORTED PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Patient Involvement
MAUDE report 7974444 ↗
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- 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.