FDA Adverse Event
Malfunction
Summary report: N
CHANNEL DRAIN
MDR report key: 24421903
·
Received February 23, 2026
Report
- Report Number
- 1018233-2026-01138
- Event Type
- Malfunction
- Date Received
- February 23, 2026
- Date of Event
- February 12, 2026
- Report Date
- April 17, 2026
- Manufacturer
- C.R. BARD INC. (COVINGTON) -1018233
- Product Code
- GBX
- PMA / PMN Number
- EXEMPT
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IL, US
- Reporter Occupation
- PHYSICIAN
- Health Professional
- Yes
Narratives
Additional Manufacturer Narrative · 0
THE INITIAL REPORTER'S FACILITY NAME: (B)(6). THE INVESTIGATION IS STILL IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETE, A SUPPLEMENTAL REPORT WILL BE FILED. UDI FORMAT UPDATED WITH AVAILABLE PRODUCT INFORMATION PER GUDID. H11: SECTIONS A THROUGH F - THE INFORMATION PROVIDED BY BD REPRESENTS ALL THE KNOWN INFORMATION AT THIS TIME. DESPITE GOOD FAITH EFFORTS TO OBTAIN ADDITIONAL INFORMATION, THE COMPLAINANT / REPORTER WAS UNABLE OR UNWILLING TO PROVIDE ANY FURTHER PATIENT, PRODUCT, OR PROCEDURAL DETAILS TO BD.
Description of Event or Problem · 0
THEY STATED THAT PIECES OF SILICONE OF ITEM: 072223 WERE FLAKING OFF.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 475712 | CHANNEL DRAIN | WOUND DRAIN | GBX | C.R. BARD INC. (COVINGTON) -1018233 | NGKX2316 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Female | Other |