ARROW PICC SET 2-LUMEN: 5 FR X 19-5/8" (50 CM)
Report
- Report Number
- 9680794-2022-00236
- Event Type
- Malfunction
- Date Received
- April 19, 2022
- Date of Event
- March 28, 2022
- Report Date
- March 28, 2022
- Manufacturer
- ARROW INTERNATIONAL LLC
- Product Code
- LJS
- PMA / PMN Number
- K042126
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CO
- Reporter Occupation
- OTHER
- Health Professional
- N
Narratives
(B)(4).
(B)(4). COMPLAINT VERIFICATION TESTING COULD NOT BE PERFORMED AS IT WAS REPORTED THAT THE SAMPLE IS NOT AVAILABLE FOR RETURN. A DEVICE HISTORY RECORD REVIEW WAS PERFORMED AND NO RELEVANT FINDINGS WERE IDENTIFIED. WITHOUT THE DEVICE TO EVALUATE THE COMPLAINT COULD NOT BE CONFIRMED AND THE PROBABLE CAUSE COULD NOT BE DETERMINED FROM THE AVAILABLE INFORMATION. TELEFLEX WILL CONTINUE TO MONITOR AND TREND FOR REPORTS OF THIS NATURE.
THE COMPLAINT IS REPORTED AS: "TWO ATTEMPTS ARE MADE TO INSERT PERIPHERALLY INSERTED CENTRAL CATHETER IN THE LEFT AND RIGHT UPPER LI MBS, RETURN IS OBTAINED BUT THE GUIDE IS BENT AT THE AXILLARY LEVEL, THE DOCTOR ON DUTY IS INFORMED, WHO ORDERS CENTRAL CATHETER INSERTION." NO PATIENT HARM WAS REPORTED. THE PATIENT'S CONDITION IS REPORTED AS FINE.
THE COMPLAINT IS REPORTED AS: "TWO ATTEMPTS ARE MADE TO INSERT PERIPHERALLY INSERTED CENTRAL CATHETER IN THE LEFT AND RIGHT UPPER LI MBS, RETURN IS OBTAINED BUT THE GUIDE IS BENT AT THE AXILLARY LEVEL, THE DOCTOR ON DUTY IS INFORMED, WHO ORDERS CENTRAL CATHETER INSERTION." NO PATIENT HARM WAS REPORTED. THE PATIENT'S CONDITION IS REPORTED AS FINE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2619655 | ARROW PICC SET 2-LUMEN: 5 FR X 19-5/8" (50 CM) | CATHETER, INTRAVASCULAR, THER | LJS | ARROW INTERNATIONAL LLC | 14F21G0057 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Female | N/A.| N/A. |