FDA Adverse Event
Injury
Summary report: N
SWEET TIP
MDR report key: 2780606
·
Received October 10, 2012
Report
- Report Number
- 2124215-2012-13436
- Event Type
- Injury
- Date Received
- October 10, 2012
- Date of Event
- September 13, 2012
- Report Date
- September 13, 2012
- Manufacturer
- CPI - DEL CARIBE
- Product Code
- NVN
- PMA / PMN Number
- K893957
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- PHYSICIAN
Narratives
Additional Manufacturer Narrative · 1
THE SYSTEM WAS SUCCESSFULLY REPLACED. AS NO FURTHER INFORMATION CONCERNING THIS REPORT IS EXPECTED, OUR INVESTIGATION IS COMPLETE. THIS INVESTIGATION WILL BE UPDATED SHOULD FURTHER INFORMATION BE PROVIDED.
Description of Event or Problem · 1
BOSTON SCIENTIFIC RECEIVED INFORMATION THAT THIS PRODUCT WAS PART OF A SYSTEM REVISION DUE TO INFECTION. THERE WERE NO ADDITIONAL ADVERSE EFFECTS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SWEET TIP | IMPLANTABLE LEAD | NVN | CPI - DEL CARIBE | 4269 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 69 YR | Hospitalization| L| R | 1821| 0015| 4269| 0095| T177| 0125| 1810 |