FDA Adverse Event
Injury
Summary report: N
SYNCHROMED II
MDR report key: 1892411
·
Received November 3, 2010
Report
- Report Number
- 3004209178-2010-08788
- Event Type
- Injury
- Date Received
- November 3, 2010
- Date of Event
- October 5, 2010
- Report Date
- October 11, 2010
- Manufacturer
- MDT PUERTO RICO OPERATIONS CO., JUNCOS
- Product Code
- LKK
- PMA / PMN Number
- P860004
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MN, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
(B)(4).
Description of Event or Problem · 1
IT WAS REPORTED THAT THE PATIENT'S PUMP WAS EXPLANTED AFTER APPROXIMATELY ONE MONTH DUE TO A STAPH INFECTION. THE MEDICATION BEING DELIVERED VIA THE DEVICE SYSTEM WAS NOT REPORTED. ADDITIONAL INFORMATION HAS BEEN REQUESTED, A FOLLOW-UP REPORT WILL BE SENT IF ADDITIONAL INFORMATION BECOMES AVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SYNCHROMED II | LKK | MDT PUERTO RICO OPERATIONS CO., JUNCOS | 8637-40 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 49 YR | Required Intervention | CATHETER: MODEL 8709SC, LOT# N259173004| EXPLANTED:| IMPLANTED: |