CONTIPLEX® 331706Recalls & reported problems
B. Braun Medical Inc. · Contiplex® Tuohy Tray (Kit), 18 Ga. x 4 in. Insulated Needle and Non-Stimulating Catheter (CNB400TK) · Class 2
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 04046964176982), received between Jun 19, 2019 and Jun 20, 2019 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (6 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
- Detachment of Device or Device Component6
Patient problems
- No Known Impact Or Consequence To Patient6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 20, 2019Detachment of Device or Device Component; Detachment of Device or Device Component
AS REPORTED BY THE USER FACILITY: EVENT 5: END USER REPORTS THAT THE CATHETER CONNECTORS ARE DETACHING FROM THE CATHETER. NO INJURY REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8715864 ↗MalfunctionJun 19, 2019Detachment of Device or Device Component; Detachment of Device or Device Component
AS REPORTED BY THE USER FACILITY: EVENT 3: END USER REPORTS THAT THE CATHETER CONNECTORS ARE DETACHING FROM THE CATHETER. NO INJURY REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8714490 ↗MalfunctionJun 19, 2019Detachment of Device or Device Component; Detachment of Device or Device Component
AS REPORTED BY THE USER FACILITY: EVENT 1: END USER REPORTS THAT THE CATHETER CONNECTORS ARE DETACHING FROM THE CATHETER. NO INJURY REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8714487 ↗MalfunctionJun 19, 2019Detachment of Device or Device Component; Detachment of Device or Device Component
AS REPORTED BY THE USER FACILITY: EVENT 4: END USER REPORTS THAT THE CATHETER CONNECTORS ARE DETACHING FROM THE CATHETER. NO INJURY REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8714486 ↗MalfunctionJun 19, 2019Detachment of Device or Device Component; Detachment of Device or Device Component
AS REPORTED BY THE USER FACILITY: EVENT 6: END USER REPORTS THAT THE CATHETER CONNECTORS ARE DETACHING FROM THE CATHETER. NO INJURY REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8714485 ↗MalfunctionJun 19, 2019Detachment of Device or Device Component; Detachment of Device or Device Component
AS REPORTED BY THE USER FACILITY: EVENT 2: END USER REPORTS THAT THE CATHETER CONNECTORS ARE DETACHING FROM THE CATHETER. NO INJURY REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8714484 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.