Kangaroo 702505Recalls & reported problems
Cardinal Health, Inc. · Gravity Feeding Bag,Large Bore · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10884521002197), received between Jul 25, 2019 and Apr 29, 2021 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (3 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 Leak3
- Detachment of Device or Device Component1
Patient problems
- Insufficient Information1
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 29, 2021Fluid/Blood Leak; Fluid/Blood Leak
CUSTOMER REPORTS: GRAVITY BAGS ARE LEAKING.
Patient problems: Insufficient Information
MAUDE report 11745518 ↗MalfunctionJan 21, 2020Fluid/Blood Leak; Fluid/Blood Leak
THE CUSTOMER REPORTED BOTH FORMULA AND POTENTIALLY STOMACH ACID LEAKED ON TO THE PATIENT FROM WHERE THE LUER LOCK TYPE CONNECTION ATTACHES TO THE G-TUBE. THERE WERE NO BURNS OBSERVED. THE TUBING DID NOT SEEM TO DISCONNECT FROM THE LUER LOCK PORT AS BOTH PIECES WERE STILL INTACT. IN ADDITION, THE CUSTOMER DOES NOT HAVE THE LOT NUMBER AVAILABLE AND DOES NOT HAVE THE AFFECTED PRODUCT AS IT WAS DISCARDED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9611390 ↗MalfunctionJul 25, 2019Fluid/Blood Leak; Detachment of Device or Device Component; Fluid/Blood Leak; Detachment of Device or Device Component
THE CUSTOMER REPORTS THAT WHILE GETTING THE TUBE FEEDING READY, THE CONNECTOR CAME APART WHERE IT MEETS THE TUBE CAUSING LEAKING. A NEW SET WAS USED AND THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8826019 ↗
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- 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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