Kangaroo 762010ERecalls & reported problems
Cardinal Health 200, LLC · Saftey Single Pass Peg Kit With ENFit™ Connection · Class 2 · Implant
All models of Kangaroo (35)
Data updated Oct 16, 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 10192253009606), received between Mar 27, 2025 and Mar 27, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- Foreign Body In Patient1
- Pain1
- Pneumoperitoneum1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 27, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THERE WAS A PIECE THAT BROKE OFF AND THERE WAS ALSO ADDITIONAL RIGIDITY TO ONE OF THE PIECES ON THE TUBE THAT SEEMED TO BE ABNORMAL. PER ADDITIONAL INFORMATION PROVIDED BY THE REPORTER, THE PRODUCT ISSUES WERE DISCOVERED ON (B)(6) 2025 WHEN THE PATIENT WENT INTO THE OFFICE FOR REMOVAL. REMOVAL WAS ATTEMPTED BUT WAS UNSUCCESSFUL, REQUIRING EGD (ESOPHAGOGASTRODUODENOSCOPY) PROCEDURE. BOTH THE TUBE AND INTERNAL BUMPER HAD ADDITIONAL RIGIDITY. THE INTERNAL BUMPER POPPED/BROKE OFF THE TUBING RESULTING IN A FOREIGN BODY THAT WAS NOTED DURING THE EGD FOR REMOVAL. REMOVAL OF THE FOREIGN BODY WAS PERFORMED ON (B)(6) 2025 BY (B)(6) VIA GASTROSCOPE. THE PATIENT EXPERIENCED POST PROCEDURE PAIN REQUIRING AN ER VISIT AND TWO-DAY HOSPITAL ADMISSION RELATED TO PNEUMOPERITONEUM. MEDICAL TREATMENT INCLUDED PAIN CONTROL, IV ANTIBIOTICS, AND REPEAT SCANS TO MONITOR PNEUMOPERITONEUM.
Patient problems: Foreign Body In Patient; Pain; Pneumoperitoneum
MAUDE report 21707509 ↗
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
- 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
- NutraGlide Nasal Feeding Tube ENFT-06055-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 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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