FDA Recall Terminated

BodyGuardian Heart Remote Monitoring Kit, consisting of two BG Heart monitors, either Models BC-1001-A or BC1001-D, and a cell phone, either Models BP1008 or BP10014, that is paired to both of the monitors.

Recall: Z-2479-2020 · Initiated August 6, 2019

Recall

Recall Number
Z-2479-2020
Event Number
85233
Firm
Preventice Services, LLC
FEI Number
3005332083
Product Code
DSI
Status
Terminated
Root Cause
Software design (manufacturing process)
Initiated
August 6, 2019
Terminated
November 18, 2022
Address
1717 N Sam Houston Pkwy W, Ste 100, Houston, TX, 77038-1324

Description

BodyGuardian Heart Remote Monitoring Kit, consisting of two BG Heart monitors, either Models BC-1001-A or BC1001-D, and a cell phone, either Models BP1008 or BP10014, that is paired to both of the monitors.

Reason

The device data being collected and transferred to the monitoring center may not be accurate due to nonvalidated association between the phone software and the heart monitors, therefore, the patient's report should not be used to evaluate their condition.

Action

On 8/6/2019, the recalling firm contacted or attempted to contact by phone all patients that had potentially impacted devices. Phone communication to the physicians of the patients also began on 8/6/2019. All patients that agreed were sent new devices to replace the affected one to finish their study.

Distribution

US Nationwide Distribution to AK, AL, GA, NJ, OH, and TX. There was no foreign/military/government distribution.

Quantity

8 kits