FDA Adverse Event
Malfunction
Summary report: N
CAPSUREFIX NOVUS
MDR report key: 3991481
·
Received August 8, 2014
Report
- Report Number
- 2649622-2014-08080
- Event Type
- Malfunction
- Date Received
- August 8, 2014
- Date of Event
- March 26, 2014
- Report Date
- May 12, 2014
- Manufacturer
- MPRI
- Product Code
- DTB
- PMA / PMN Number
- P930039
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MO, US
- Reporter Occupation
- HEALTH PROFESSIONAL
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. CONCOMITANT MEDICAL PRODUCTS: VEDR01 IPG, IMPLANTED: (B)(6) 2009. (B)(4).
Description of Event or Problem · 1
IT WAS LATER REPORTED THAT THE LEAD HAD INFINITE IMPEDANCE.
Description of Event or Problem · 1
IT WAS REPORTED THAT THE ATRIAL LEAD HAD HIGH IMPEDANCE THAT TRIGGERED A LEAD WARNING. SOME OVERSENSING WAS ALSO OBSERVED. 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 |
|---|---|---|---|---|---|---|---|
| 471094 | CAPSUREFIX NOVUS | ELECTRODE, PACEMAKER, PERMANENT | DTB | MPRI | 5076-45 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 00083 YR | 5076-58 LEAD |