N/A LCB52SRecalls & reported problems
Ethicon Endo-Surgery, LLC · CHOLECYSTECTOMY TRAY
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 10705036007586), received between Jun 7, 2017 and Jun 7, 2017 — classified as 1 injury.
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
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.
InjuryJun 7, 2017Device Dislodged or Dislocated
MALFUNCTION OF THE ENDOPATH XCEL BLUNT TIP TROCHAR SUTURE TIE POST IN THAT THE POST WAS DISLOCATED FROM THE DEVICE AND UNABLE TO BE RETRIEVED FROM THE PATIENT, AND A SECOND ENDOPATH XCEL BLUNT TIP TROCHAR WAS USED AND THE POST FROM THE 2ND DEVICE WAS DISLODGED AS WELL, BUT WAS RETRIEVED PRIOR TO ENTERING THE PATIENT. THE FIRST TROCHAR WAS IN THE FLEXTRAY PROCEDURE DELIVERY SYSTEM. THE SECOND TROCHAR WAS SEPARATE.
Patient problems: Foreign Body In Patient
MAUDE report 6629602 ↗
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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