CARELINK
Report
- Report Number
- 2182208-2013-01540
- Event Type
- Malfunction
- Date Received
- June 7, 2013
- Date of Event
- April 23, 2013
- Report Date
- April 23, 2013
- Manufacturer
- MEDTRONIC, INC.
- Product Code
- KRG
- PMA / PMN Number
- P890003
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MN, US
- Reporter Occupation
- OTHER
Narratives
PRODUCT EVENT SUMMARY: ANALYSIS CONFIRMED THE CUSTOMER COMMENT THAT THE PROGRAMMER HEAD HAD INTERMITTENT TELEMETRY, THE HEAD FAILED ALL UPLINK AMPLITUDE TESTS AND THE RUBBER PORTION OF THE HEAD LABEL WAS GONE. THE HEAD'S CABLE AND LABEL WERE REPLACED AND THE PROGRAMMER HEAD PASSED ALL FINAL ELECTRICAL AND BENCH SYSTEMS TEST. (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 THE RADIO FREQUENCY PROGRAMMER HEAD WAS UNABLE TO RECOGNIZE, OR INTERROGATE A PATIENT'S IMPLANTED HEART DEVICE. IT WAS NOTED THAT NUMEROUS TRIES WERE MADE. THE PROGRAMMER HEAD WAS RETURNED FOR SERVICE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.
IT WAS REPORTED THAT THE RADIO FREQUENCY PROGRAMMER HEAD WAS UNABLE TO RECOGNIZE, OR INTERROGATE A PATIENT'S IMPLANTED HEART DEVICE. IT WAS NOTED THAT NUMEROUS TRIES WERE MADE. THE PROGRAMMER HEAD WAS RETURNED FOR SERVICE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 253203 | CARELINK | PROGRAMMER, PACEMAKER | KRG | MEDTRONIC, INC. | 2067L |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |