Contiplex® 331768Recalls & reported problems
B. Braun Medical Inc. · Contiplex® Echo Set, Closed-tip Echogenic Catheter with 18 Ga. x 4 in. Insulated Echogenic Tuohy (CNB400TU3EC) · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04046964991431), received between Aug 27, 2025 and Aug 27, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 27, 2025Break; Break
AS REPORTED BY THE USER FACILITY: DETAILED INQUIRY DESCRIPTION: "WHILE THE DR HAD THE NEEDLE THREADED IN THE CATHETER, HE PULLED BACK ON THE CATHETER TO POSITION IT AND BEGAN TO SEPARATE. THE CATHETER DID NOT FULLY SEPARATE OR BREAK INTO MULTIPLE PIECES. HE WAS ABLE TO SUCCESSFULLY RETRIEVE ALL PIECES OF THE CATHETER USING C-ARM XRAY VERIFICATION AND SUBSEQUENTLY THERE WAS NO HARM TO THE PATIENT. ".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22905630 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.