Endo Babcock 174001Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10884523000795), received between Jul 26, 2018 and Feb 4, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Break” (2 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 4, 2026Break; Detachment of Device or Device Component; Physical Resistance/Sticking

  IT WAS REPORTED THAT DURING A PROCEDURE, THE HANDLES BOUND WHILE THE DEVICE WAS CLAMPED ON TISSUE, THE FRONT OF THE DEVICE FRACTURED, AND FRAGMENTS FELL OFF THE DEVICE. THE DEVICE WAS REPLACED. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24258839 ↗
• MalfunctionAug 12, 2020Difficult to Open or Close; Difficult to Open or Close

  ACCORDING TO THE REPORTER, DURING A LAPAROSCOPIC RIGHT HEMICOLECTOMY, ON CLAMPING THE BOWEL, THE DEVICE COULD NOT CLOSE ITS JAW. ANOTHER PRODUCT WAS USED TO COMPLETE THE CASE. THERE WAS NO PATIENT INJURY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10396275 ↗
• MalfunctionJul 26, 2018Break

  ACCORDING TO THE REPORTER, DURING A LAPAROSCOPIC COLON RESECTION, THE DEVICE BROKE. THEY USED ANOTHER DEVICE TO COMPLETE THE CASE. THERE WAS NO PATIENT INJURY.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7722925 ↗