FDA Adverse Event
Malfunction
Summary report: N
ZEPHYR XL DR
MDR report key: 4202241
·
Received January 13, 2014
Report
- Report Number
- 2017865-2014-05012
- Event Type
- Malfunction
- Date Received
- January 13, 2014
- Date of Event
- April 12, 2012
- Manufacturer
- ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI
- Product Code
- LWP
- PMA / PMN Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CT, US
- Reporter Occupation
- PHYSICIAN
Narratives
Additional Manufacturer Narrative · 1
ALL INFORMATION PROVIDED BY MANUFACTURER, NO MEDWATCH FORM WAS RECEIVED. THIS HISTORICAL COMPLAINT IS BEING FILED AS PART OF A RETROSPECTIVE REVIEW OF COMPLAINT FILES IN RESPONSE TO A RECENT FDA INSPECTION. THERE IS NO CHANGE TO THE ACTUAL PERFORMANCE OF THE PRODUCT AND THIS REPORT ONLY REPRESENTS AN ENHANCEMENT TO THE REPORTING CRITERIA GOING FORWARD. EVALUATION DESCRIPTION: ANALYSIS WAS NORMAL. NO ANOMALY WAS DETECTED. (B)(4).
Description of Event or Problem · 1
IT WAS REPORTED THAT BOTH PACING LEAD IMPEDANCES WERE OUT OF RANGE THROUGH THE PULSE GENERATOR AND WOULD NOT CAPTURE WITH BIPOLAR PULSE CONFIGURATION. THE LEAD WAS NOT IMPLANTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 28380 | ZEPHYR XL DR | IMPLANTABLE PACEMAKER PULSE GENERATOR, | LWP | ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI | 5820 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 83 YR |