FDA Adverse Event
Injury
Summary report: N
CAPSURE SP NOVUS
MDR report key: 3152584
·
Received June 7, 2013
Report
- Report Number
- 2649622-2013-06736
- Event Type
- Injury
- Date Received
- June 7, 2013
- Date of Event
- February 3, 2013
- Report Date
- March 1, 2013
- Manufacturer
- MPRI
- Product Code
- DTB
- PMA / PMN Number
- P850089
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- DE, 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. CONCOMITANT PRODUCTS: 5092-58 IMPLANTABLE PACING LEAD (B)(6) 2013; ADDRL1 IMPLANTABLE PULSE GENERATOR (B)(6) 2013. (B)(4).
Description of Event or Problem · 1
IT WAS REPORTED THAT THE PATIENT FELT 'SYMPTOMATIC' THREE DAYS POST-IMPLANT AT THE PHYSICIAN'S OFFICE. THE RIGHT ATRIAL AND RIGHT VENTRICULAR LEADS HAD PULLED BACK. BOTH LEADS WERE REPOSITIONED. NO FURTHER PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 252060 | CAPSURE SP NOVUS | ELECTRODE, PACEMAKER, PERMANENT | DTB | MPRI | 5592-53 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 00075 YR | Hospitalization| R |