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Reddick Scoop Tip Cholangiogram Catheter e2401-51Recalls & reported problems

Lemaitre Vascular, Inc. · Reddick Scoop Tip Cholangiogram Stiffer Catheter, 4F, eIFU · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00840663101818), received between Jan 9, 2020 and Feb 11, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Difficult to Insert” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Difficult to Insert2
  • Material Deformation1

Patient problems

  • No Known Impact Or Consequence To Patient2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 11, 2020Difficult to Insert; Material Deformation

    DURING A LAPAROSCOPIC CHOLECYSTECTOMY WITH INTRAOPERATIVE CHOLANGIOGRAM. THE CHOLANGIOGRAM CATHETER TIP BUBBLED UP AT THE END AND COULD NOT BE INSERTED. A NEW CATHETER HAD TO BE OPENED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9695915 ↗
  • MalfunctionJan 9, 2020Difficult to Insert

    THE CHOLANGIOGRAM CATHETER TIP BUBBLED UP AT THE END AND COULD NOT BE INSERTED. A NEW CATHETER HAD TO BE OPENED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9568647 ↗

Other Catheter, Cholangiography devices

All Catheter, Cholangiography devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.