ATTAIN OTW
Report
- Report Number
- 2649622-2011-02991
- Event Type
- Injury
- Date Received
- February 15, 2011
- Manufacturer
- MEDTRONIC PUERTO RICO, INC.
- Product Code
- DTB
- PMA / PMN Number
- P010015/S012
- Removal / Correction Number
- ASKU
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- PHYSICIAN
Narratives
THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. EVALUATION SUMMARY (B)(4) DEVICE DID NOT MEET EXPECTED LONGEVITY.
ASKU
IT WAS REPORTED THE PATIENT WAS EXPERIENCING DIAPHRAGMATIC STIMULATION. THE LV AMPLITUDE WAS DECREASED "WITH GOOD RESULTS." NO FURTHER PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT. IT WAS LATER REPORTED THE LEFT VENTRICULAR LEAD AND DEVICE WERE EXPLANTED AND REPLACED. THE DEVICE WAS RETURNED TO MANUFACTURER, ANALYZED, AND SUBSEQUENTLY TESTED OUT OF SPECIFICATION. LATER REPORTED THE LEFT VENTRICULAR LEAD WAS EXPLANTED DUE TO "NON FUNCTIONAL."
IT WAS REPORTED THE PATIENT WAS EXPERIENCING DIAPHRAGMATIC STIMULATION. THE LV AMPLITUDE WAS DECREASED "WITH GOOD RESULTS." NO FURTHER PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT. THE LEFT VENTRICULAR LEAD AND DEVICE WERE EXPLANTED AND REPLACED. THE DEVICE WAS RETURNED TO MANUFACTURER, ANALYZED, AND SUBSEQUENTLY TESTED OUT OF SPECIFICATION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ATTAIN OTW | IMPLANTABLE PACING LEAD | DTB | MEDTRONIC PUERTO RICO, INC. | 4194 | ASKU |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 47 YR | Hospitalization| R | 6949 IMPLANTABLE TACHY LEAD| 6949 IMPLANTABLE TACHY LEAD| 5076 IMPLANTABLE PACING LEAD| 5076 IMPLANTABLE PACING LEAD |