Channel Drain 072186Recalls & reported problems
C. R. Bard, Inc. · Channel Drain, 10 Fr. Round Full Fluted · Class 1
All models of Channel Drain (27)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 00801741049682), received between Aug 13, 2025 and Aug 13, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Defective Device” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Defective Device1
- Device Contamination with Chemical or Other Material1
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 13, 2025Defective Device; Device Contamination with Chemical or Other Material; Defective Device; Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT THE CUSTOMER STATED THAT THEY HAVE RECEIVED ADDITIONAL COMPLAINTS WITH THAT WOUND DRAIN, AS WELL AS IDENTIFIED THAT THIS MAY AFFECT MULTIPLE ITEMS NOT JUST THE ORIGINALLY REPORTED. THEY NEED TO SET UP A CALL, TO DISCUSS OVER THAT ISSUE. THEY WERE LOOKING AT REMOVING THAT PRODUCT AND OTHERS FROM INVENTORY TILL THEY HAVE AN ALL CLEAR. THEY MENTIONED IMPACTED MATERIAL BELOW: MATERIAL #072211, MATERIAL #072190, MATERIAL #072189, MATERIAL #072214, MATERIAL #072186.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22794110 ↗
Other CATHETER, IRRIGATION devices
- Navarre Opti-Drain NOD8LPTBard Access Systems, Inc. · CATHETER, IRRIGATION901 reports
- Navarre NNU8LPTBard Access Systems, Inc. · CATHETER, IRRIGATION736 reports
- BLAKE 2227Ethicon Inc. · CATHETER, IRRIGATION331 reports
- Navarre NNU6LPTBard Access Systems, Inc. · CATHETER, IRRIGATION211 reports
- Navarre Opti-Drain NOD10LPTBard Access Systems, Inc. · CATHETER, IRRIGATION178 reports
- Navarre NNU10LPTBard Access Systems, Inc. · CATHETER, IRRIGATION127 reports
- BLAKE 2233Ethicon Inc. · CATHETER, IRRIGATION114 reports
- Vasoshield VH-5001Maquet Cardiovascular LLC · Catheter, Irrigation1 recall27 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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