FDA Adverse Event Injury Summary report: N

LIFEVEST WCD 4000 SYSTEM

MDR report key: 4564916 · Received February 27, 2015

Report

Report Number
3008642652-2015-00994
Event Type
Injury
Date Received
February 27, 2015
Date of Event
January 31, 2015
Report Date
February 25, 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

Additional Manufacturer Narrative · 1

THERE WAS NOT DEATH OR DEVICE MALFUNCTION ASSOCIATED WITH THE INAPPROPRIATE DEFIBRILLATION. THERE IS NO INFORMATION TO SUGGEST THAT THE PT SUSTAINED A SERIOUS INJURY. THE PT DID NOT SEEK MEDICAL ATTENTION 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): 10/2014 - REUSE, ELECTRODE BELT (B)(4): 09/2014 - INITIAL USE.

Description of Event or Problem · 1

A US DISTRIBUTOR CONTACTED ZOLL TO REPORT THAT A PT EXPERIENCED AN INAPPROPRIATE DEFIBRILLATION EVENT. MULTIPLE COUNTING CONTRIBUTED TO THE FALSE DETECTION. THE PT WAS REPORTEDLY CONSCIOUS AT THE TIME OF THE EVENT AND REPORTED THAT HE PRESSED THE RESPONSE BUTTONS. REVIEW OF THE PT'S DOWNLOADED DATA REVEALS THAT THE RESPONSE BUTTONS WERE PRESSED DURING AN EARLIER DETECTION, BUT NOT DURING THE DEFIBRILLATION EVENT. THE RESPONSE BUTTONS WERE ALSO FUNCTIONAL DURING THE SUBSEQUENT POWER ON SEQUENCE. THE RESPONSE BUTTONS FUNCTIONED APPROPRIATELY. THE PT DID NOT SEEK MEDICAL ATTENTION AND CONTINUED USE OF THE LIFEVEST.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
140961 LIFEVEST WCD 4000 SYSTEM WEARABLE CARDIOVERTER DEFIBRILALTOR MVK ZOLL MANUFACTURING CORP WCD 4000 NA

Patients

Seq Age Sex Outcome Treatment
1 70 YR Other