LIFEVEST WCD 4000 SYSTEM
Report
- Report Number
- 3008642652-2015-00898
- Event Type
- Injury
- Date Received
- February 27, 2015
- Date of Event
- February 1, 2015
- Report Date
- February 23, 2015
- Manufacturer
- ZOLL MANUFACTURING CORP
- Product Code
- MVK
- PMA / PMN Number
- P010030
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
THERE WAS NO DEATH OR DEVICE MALFUNCTION ASSOCIATED WITH THE INAPPROPRIATE DEFIBRILLATION. THERE IS NO INFORMATION TO SUGGEST THAT THE PT SUSTAINED A SERIOUS INJURY. THE PT VISITED THE CLINIC FOR FURTHER EVALUATION AND CONTINUED USE OF THE LIFEVEST. DEVICE EVALUATION WAS ACCOMPLISHED THROUGH A REVIEW OF THE PT'S DOWNLOADED DATA FILE. REVIEW OF THE DATA DOES NOT INDICATE ANY DEVICE MALFUNCTION RELATED TO THE DEFIBRILLATION EVENT. MONITOR (B)(4): 12/2013, ELECTRODE BELT (B)(4): 03/2012. INAPPROPRIATE DEFIBRILLATIONS ARE AN ANTICIPATED RISK ASSOCIATED WITH THE USE OF THE LIFEVEST. PTS ARE INSTRUCTED THROUGH ALARMS, VOICE MESSAGES, IFU, AND TRAINING TO PRESS THE RESPONSE BUTTONS TO PREVENT AN INAPPROPRIATE DEFIBRILLATION. (B)(4).
A US DISTRIBUTOR CONTACTED ZOLL TO REPORT THAT A (B)(6) PT EXPERIENCED AN INAPPROPRIATE DEFIBRILLATION EVENT WHILE RUNNING FOR A TRAIN. MOTION ARTIFACT CONTRIBUTED TO THE FALSE DETECTION. THE PT WAS REPORTEDLY CONSCIOUS DURING THE EVENT. THE RESPONSE BUTTONS WERE NOT PRESSED DURING THE ENTIRE EVENT. THE PT VISITED THE CLINIC FOR FURTHER EVALUATION AND CONTINUED USE OF THE LIFEVEST.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 140594 | LIFEVEST WCD 4000 SYSTEM | WEARABLE CARDIOVERTER DEFIBRILLATOR | MVK | ZOLL MANUFACTURING CORP | WCD 4000 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 58 YR | Other |