COUPLER
Report
- Report Number
- 1416980-2019-00666
- Event Type
- Injury
- Date Received
- February 8, 2019
- Report Date
- March 7, 2019
- Manufacturer
- BAXTER HEALTHCARE - SAINT PAUL - MCA
- Product Code
- MVR
- PMA / PMN Number
- K861985
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AL, US
- Reporter Occupation
- OTHER
Narratives
ADDITIONAL INFORMATION: THE DEVICE WAS NOT RETURNED AND THE LOT NUMBER IS UNKNOWN; THEREFORE, A DEVICE ANALYSIS COULD NOT BE COMPLETED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.
C JALOUX, B. BETRAND, A. MAYOLY, M. CEGARRA-ESCOLANO, C. PHILANDRIANOS. MICROVASCULAR ANASTOMOTIC COUPLER: AN UNEXPECTED ADVERSE EVENT, THIEME E-JOURNALS-JOURNAL OF RECONSTRUCTIVE MICROSURGERY/ABSTRACT, OCULOPLASTIC SURGERY, THIRD EDITION, HTTPS://WWW.THIEME-CONNECT.DE/MEDIA/IRM/EFIRST/LOOKINSIDE/10-1055-S-0038-1677036-180263-1.IPG. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.
IT WAS REPORTED THAT A PATIENT UNDERWENT A REVISION SURGERY TO REMOVE A 1.5MM COUPLER DEVICE WHICH WAS USED FOR AN ANASTOMOSIS BETWEEN THE ANTEROLATERAL THIGH (ALT) PEDICLE VEINS AND THE DORSALIS PEDIS VEINS. IT WAS REPORTED APPROXIMATELY NINE MONTHS AFTER THE INITIAL SURGERY, THE PATIENT COMPLAINED OF A SMALL DISCOMFORT IN THE DORSUM OF THE OPERATED FOOT. AN X-RAY WAS PERFORMED WHICH CONFIRMED THE DEVICE UNDERNEATH THE SKIN. THE REVISION SURGERY REMOVED THE DEVICE AND THE ARTERY WAS LEFT ANASTOMOSED. IT WAS REPORTED THERE WERE NO COMPLICATIONS AFTER THE PROCEDURE. NO ADDITIONAL INFORMATION IS AVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 115100 | COUPLER | DEVICE, ANASTOMOTIC, MICROVASCULAR | MVR | BAXTER HEALTHCARE - SAINT PAUL - MCA | NA | NI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 60 YR | Required Intervention | COUPLER 2.0MM |