PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE
Report
- Report Number
- 2183613-2013-00676
- Event Type
- Malfunction
- Date Received
- June 7, 2013
- Date of Event
- April 17, 2013
- Report Date
- April 17, 2013
- Manufacturer
- MEDTRONIC MILACA, INC.
- Product Code
- LWP
- PMA / PMN Number
- P820003
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- VA, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
PRODUCT EVENT SUMMARY: ANALYSIS CONFIRMED THE CUSTOMER COMMENT THAT THE ATRIAL OUTPUT CONNECTOR WAS OCCLUDED BY A STUCK PIN. ANALYSIS ALSO DETERMINED THAT THE UPPER AND LOWER CASES AND BOTH BAIL COVERS WERE BROKEN, THE BATTERY CONTACTS COMPRESSED AND THE SERIAL NUMBER LABEL DAMAGED. (B)(4).
THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. (B)(4).
IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
IT WAS REPORTED THAT THERE WAS A PIN STUCK IN THE ATRIAL PORT OF THE EXTERNAL PULSE GENERATOR. THE GENERATOR WAS RETURNED FOR SERVICE. IT WAS INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT ASSOCIATED WITH THIS EVENT.
IT WAS REPORTED THAT THERE WAS A PIN STUCK IN THE ATRIAL PORT OF THE EXTERNAL PULSE GENERATOR. THE GENERATOR WAS RETURNED FOR SERVICE. IT WAS INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT ASSOCIATED WITH THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 252980 | PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE | LWP | MEDTRONIC MILACA, INC. | 5388 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |