FDA Adverse Event
Malfunction
Summary report: N
ZEPHYR XL DR
MDR report key: 1896411
·
Received November 10, 2010
Report
- Report Number
- 2017865-2010-05354
- Event Type
- Malfunction
- Date Received
- November 10, 2010
- Date of Event
- August 31, 2010
- Manufacturer
- ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
- Product Code
- DXY
- PMA / PMN Number
- P880086
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Additional Manufacturer Narrative · 1
ALL INFORMATION PROVIDED BY MANUFACTURER, NO MEDWATCH FORM WAS RECEIVED. COMPANY SALES REPRESENTATIVE.
Description of Event or Problem · 1
IT WAS REPORTED THAT PRIOR TO OPENING THE BOX, ATTEMPTS TO INTERROGATE THE PULSE GENERATOR WERE UNSUCCESSFUL. ATTEMPTS TO INTERROGATE THE DEVICE OUT OF THE BOX, USING TWO DIFFER- ENT PROGRAMMERS AGAIN FAILED. THE DEVICE WAS NOT IMPLANTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ZEPHYR XL DR | IMPLANTABLE PACEMAKER PULSE GENERATOR | DXY | ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION | 5826 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |