EPIDURAL CATHETERIZATION KIT
Report
- Report Number
- 1036844-2020-00106
- Event Type
- Malfunction
- Date Received
- March 12, 2020
- Date of Event
- February 24, 2020
- Report Date
- February 25, 2020
- Manufacturer
- ARROW INTERNATIONAL INC.
- Product Code
- BSO
- PMA / PMN Number
- K140110
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- RISK MANAGER
Narratives
QN#(B)(4). A DEVICE HISTORY RECORD REVIEW WAS PERFORMED ON THE EPIDURAL CATHETER AND NEEDLE WITH NO RELEVANT FINDINGS. A CORRECTIVE ACTION IS NOT REQUIRED AT THIS TIME AS A POTENTIAL ROOT CAUSE COULD NOT BE DETERMINED BASED UPON THE INFORMATION PROVIDED AND WITHOUT A SAMPLE. COMPLAINT VERIFICATION TESTING COULD NOT BE PERFORMED AS NO SAMPLE WAS RETURNED FOR ANALYSIS. A DEVICE HISTORY RECORD REVIEW WAS PERFORMED ON THE EPIDURAL CATHETER AND NEEDLE WITH NO EVIDENCE TO SUGGEST A MANUFACTURING RELATED CAUSE. THE POTENTIAL CAUSE OF THE CATHETER KINKING DURING USE COULD NOT BE DETERMINED BASED UPON THE INFORMATION PROVIDED AND WITHOUT A SAMPLE.
IT WAS REPORTED THAT A PLETHORA OF CATHETERS KINK BADLY DURING INSERTION AND COULD NOT PASS THROUGH THE NEEDLE. THERE WAS NO PATIENT INJURY.
(B)(4). THE DEVICE HAS NOT BEEN RETURNED FOR INVESTIGATION. TELEFLEX WILL CONTINUE TO MONITOR AND TREND RELATED EVENTS.
IT WAS REPORTED THAT A PLETHORA OF CATHETERS KINK BADLY DURING INSERTION AND COULD NOT PASS THROUGH THE NEEDLE. THERE WAS NO PATIENT INJURY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 288264 | EPIDURAL CATHETERIZATION KIT | ANESTHESIA CONDUCTION CATHETER | BSO | ARROW INTERNATIONAL INC. | 23F19L0210 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |