CARDINAL HEALTH 8884721055ERecalls & reported problems
Cardinal Health 200, LLC · ENTRIFLEX 10FR 55IN W/STYLET With ENFit Connectors · Class 2
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 10192253011739), received between Dec 16, 2025 and Dec 16, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Material Separation” (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.
Reports received per month
Most reported problems
Device problems
- Material Separation1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 16, 2025Material Separation; Material Separation
THE CUSTOMER REPORTED THE NGT WAS INSERTED IN IVR ON (B)(6) AND WAS REMOVED TODAY TO FIND A RUPTURED LOOKING TUBE WITH THE DISTAL WEIGHTED PORTION MISSING. THEY ARE WAITING ON A PLAN FOR THE PATIENT TO DETERMINE WHETHER THE PATIENT WILL HAVE A SCOPE OR WAIT AND PASS. POSSIBLE LOT NUMBER: 2519801064. PER ADDITIONAL INFORMATION PROVIDED ON DECEMBER 15TH, 2025, GASTROENTEROLOGY PERFORMED AN ESOPHAGOGASTRODUODENOSCOPY ON (B)(6) BUT THE NG TIP HAD MIGRATED BEYOND REACH. SERIAL X-RAYS AND STOOL CHARTING WERE COMPLETED TO MONITOR THE PROGRESSION OF THE NG TIP. THE FOREIGN BODY WAS REMOVED VIA COLONOSCOPY ON (B)(6) WITHOUT COMPLICATION.
Patient problems: Foreign Body In Patient
MAUDE report 23816497 ↗
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- NutraGlide Nasal Feeding Tube ENFT-06090-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- NutraGlide Nasal Feeding Tube ENFT-05090-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- Kangaroo 8884711253ECardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)100 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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