INJECTION GOLD PROBE BIPOLAR CATHETER
Report
- Report Number
- 3005099803-2008-04911
- Event Type
- Malfunction
- Date Received
- September 26, 2008
- Date of Event
- August 28, 2008
- Report Date
- August 28, 2008
- Manufacturer
- BOSTON SCIENTIFIC CORPORATION
- Product Code
- KNS
- PMA / PMN Number
- K961349
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IA, US
- Reporter Occupation
- PHYSICIAN
Narratives
A VISUAL INSPECTION OF THE DEVICE REVEALED THAT THE CATHETER WAS BENT AT THE TIP AND ALONG THE ENTIRE LENGTH OF DEVICE. A FUNCTIONAL INSPECTION OF THE DEVICE REVEALED THAT THE NEEDLE DID NOT FULLY EXTEND AND RETRACT. THE DEVICE WAS DISASSEMBLED AND THE NEEDLE / HYPOTUBE ASSEMBLY WAS FOUND TO BE BENT. THE CAUSE OF THE REPORTED MALFUNCTION IS UNK. A REVIEW OF THE DEVICE HISTORY RECORD FOR THE PERTINENT LOT WAS REVIEWED; NO ANOMALIES WERE NOTED. A SEARCH OF THE COMPLAINT DATABASE REVEALED THAT NO ADDITIONAL COMPLAINTS HAVE BEEN REPORTED FOR THE LOT.
NOTE: THIS REPORT IS FOR ONE OF THE TWO REPORTED DEVICES, REFER TO MFR #3005099803-2008-04912 FOR THE OTHER REPORT. IT WAS REPORTED TO BOSTON SCIENTIFIC THAT AN INJECTION GOLD PROBE BIPOLAR CATHETER WAS USED ON A MALE PATIENT DURING AN ESOPHAGOGASTRODUODENOSCOPY (EGD) PROCEDURE IN 2008. ACCORDING TO THE COMPLAINANT, "THE NEEDLE WOULD NOT COME OUT OR COME BACK." A SECOND INJECTION GOLD PROBE BIPOLAR CATHETER, WAS USED AND THE COMPLAINANT (PLAIN INJECTOR NEEDLE) WAS USED TO COMPLETE THE CASE (MFR UNK) WITH NO COMPLICATIONS TO THE PATIENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | INJECTION GOLD PROBE BIPOLAR CATHETER | KNS | BOSTON SCIENTIFIC CORPORATION | M00560150 | 11830354 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 88 YR |