OT PING METER
Report
- Report Number
- 2939301-2010-09977
- Event Type
- Malfunction
- Date Received
- November 17, 2010
- Report Date
- November 2, 2010
- Manufacturer
- LIFESCAN INC.
- Product Code
- NBW
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MA, US
- Reporter Occupation
- OTHER
Narratives
FOLLOW UP # 1/SUPPLEMENTAL REPORT TEXT-12/01/2010. THE LAY USER/PATIENT'S PRODUCT(S) HAS BEEN RETURNED AND EVALUATED BY LIFESCAN PRODUCT ANALYSIS WITH THE FOLLOWING FINDINGS: THE METER INVOLVED IN THIS CASE FAILED TESTING. THE METER WAS FOUND TO HAVE CRACKED/BROKEN DISPLAY. IF ANY ADDITIONAL INFORMATION IS AVAILABLE, THE FDA WILL BE NOTIFIED IN A SECOND FOLLOW UP REPORT. AT THIS TIME, WE CONSIDER THIS MATTER CLOSED.
LIFESCAN (LFS) HAS REQUESTED RETURN OF THE SUBJECT PRODUCT(S) FOR EVALUATION. IF THE PRODUCT(S) ARE RETURNED, LFS WILL EVALUATE IT/THEM AND INFORM FDA OF PRODUCT(S) THAT DO NOT PASS INSPECTION IN A SUPPLEMENTAL REPORT; 510(K)# IS K082590.
ON (B)(6) 2008, (B)(6) MALE WAS IMPLANTED WITH A GORE PROPATEN VASCULAR GRAFT IN A BYPASS PROCEDURE IN THE RIGHT LEG FROM THE COMMON FEMORAL ARTERY TO THE POPLITEAL ARTERY. ON (B)(6) 2010, THE PT PRESENTED WITH A "COMPLETELY COLLAPSED FEMORAL POPLITEAL GRAFT". A THROMBECTOMY PROCEDURE AND A GRAFT REVISION WITH A DEXON GRAFT WAS PERFORMED. ON (B)(6) 2010, THE PT PRESENTED WITH A FAILED GRAFT AND A MAJOR AMPUTATION WAS PERFORMED.
THERE IS NO INDICATION THAT THE PRODUCT CAUSED OR CONTRIBUTED TO AN ADVERSE EVENT. HOWEVER, THIS COMPLAINT IS BEING REPORTED BECAUSE BLACK MARKS WAS NOT RESOLVED WITH TROUBLESHOOTING.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | OT PING METER | GLUCOSE MONITORING SYS/KIT | NBW | LIFESCAN INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |