FDA Adverse Event
Malfunction
Summary report: N
ATLAS PLUS DR
MDR report key: 4091961
·
Received January 13, 2014
Report
- Report Number
- 2938836-2014-05139
- Event Type
- Malfunction
- Date Received
- January 13, 2014
- Date of Event
- September 25, 2012
- Manufacturer
- ST. JUDE MEDICAL, INC. CRMD
- Product Code
- LWS
- PMA / PMN Number
- P910023
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
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.
Description of Event or Problem · 1
IT WAS REPORTED THE DEVICE WAS FOUND IN SOFTWARE RESET MODE. THE DEVICE REMAINS IMPLANTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 33443 | ATLAS PLUS DR | IMPLANTABLE CARDIOVERTER DIFIBRILLATOR | LWS | ST. JUDE MEDICAL, INC. CRMD | V-243 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 73 YR |