FDA Adverse Event
Injury
Summary report: N
SPRINT QUATTRO SECURE
MDR report key: 4162967
·
Received October 10, 2014
Report
- Report Number
- 2649622-2014-12526
- Event Type
- Injury
- Date Received
- October 10, 2014
- Date of Event
- July 26, 2014
- Report Date
- July 26, 2014
- Manufacturer
- MPRI
- Product Code
- LWS
- PMA / PMN Number
- P920015
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- PHYSICIAN
Narratives
Additional Manufacturer Narrative · 1
THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. (B)(4).
Description of Event or Problem · 1
IT WAS REPORTED THAT THE RIGHT VENTRICULAR LEAD HAD OVERSENSED T WAVE PREVIOUSLY SO THE SENSITIVITY WAS PROGRAMMED TO 1.2 MILLISECONDS TO POSSIBLY PREVENT THE WAVELET FEATURE FROM SENSING T WAVES. THE PHYSICIAN DECIDED TO REPROGRAM THE WAVELET FEATURE TO MONITOR-ONLY. THE LEAD REMAINS IN USE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 639618 | SPRINT QUATTRO SECURE | DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER | LWS | MPRI | 694758 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 00031 YR | Required Intervention | D314VRG ICD |