Bard Jejunal Feeding/Gastric Decompression Tube 000733Recalls & reported problems
Bard Access Systems, Inc. · 12 Fr Tether J-Tube · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741051678), received between Jan 10, 2017 and Oct 11, 2019 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.
Most reported problems
Device problems
- Device Dislodged or Dislocated1
- Difficult to Insert1
- Material Twisted/Bent1
Patient problems
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 11, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT SOME TIME POST PLACEMENT OF THE JEJUNAL (J) TUBE THROUGH THE PERCUTANEOUS ENDOSCOPIC GASTROSTOMY (PEG) TUBE, THE PATIENT ALLEGEDLY EXPERIENCED ABDOMINAL DISTENSION AND THE JEJUNAL TUBE WAS PUSHED FOUR INCHES AWAY FROM THE STOMACH. REPORTEDLY, THE DEVICE WAS REMOVED AND REPLACED. DURING THE DEVICE REMOVAL PROCEDURE, IT WAS FOUND THAT THE JEJUNAL TUBE WAS INTERTWINED WITH THE PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TUBE. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9182549 ↗InjuryJan 10, 2017Difficult to Insert; Material Twisted/Bent
ON 12/21/2016- PER MEDWATCH REPORT, THE FACILITY REPORTED, "JEJUNOSTOMY FEEDING TUBE WAS BEING INSERTED THROUGH AN EXISTING GASTROSTOMY TUBE VIA ENDOSCOPY. PATIENT HAD TUMOR BURDEN AT THE GASTRIC OUTLET AND TUBE WAS DIFFICULT TO PLACE. THE GUIDEWIRE BECAME TANGLED AROUND THE DISTAL END OF THE TUBE. ATTEMPTS TO WITHDRAW THE TUBE VIA ENDOSCOPY WERE UNSUCCESSFUL. PATIENT TRANSFERRED TO INTERVENTIONAL RADIOLOGY FOR TUBE EXTRACTION. THEY SUCCESSFULLY WITHDREW THE TUBE AND GUIDEWIRE, BUT DISTAL END OF THE TUBE,WITH THE WEIGHT ,SHEERED OFF AND REMAINED LODGED IN THE GASTRIC OUTLET. PATIENT TRANSFERRED BACK TO GI LAB AND DISTAL WEIGHTED TUBE END WAS REMOVED BY ENDOSCOPY".
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6238913 ↗
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-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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