FDA Recall Open, Classified

BioButton REF BIOST06040 with Software version 3.0.20 The BioButton System is a remote monitoring wearable device intended for continuous collection of physiological data in home and healthcare settings while the patient is at rest.

Recall: Z-2616-2024 · Initiated July 19, 2024

Recall

Recall Number
Z-2616-2024
Event Number
94943
Firm
Biointellisense Inc. 570 El Camino Real
FEI Number
3016592682
Product Code
DRG
Status
Open, Classified
Root Cause
Device Design
Initiated
July 19, 2024
Posted
August 14, 2024
Address
Ste 200, Redwood City, CA, 94063-1248

Description

BioButton REF BIOST06040 with Software version 3.0.20 The BioButton System is a remote monitoring wearable device intended for continuous collection of physiological data in home and healthcare settings while the patient is at rest.

Reason

Software anomaly causing the skin temperature measurement accuracy to be slightly out of specification.

Action

On 07/19/2024, the firm sent an "URGENT: MEDICAL DEVICE CORRECTION" Letter to customers informing them of a software anomaly that may cause the skin temperature accuracy to be slightly out of specification. Customers are instructed to: - (For customers who wish to receive remote firmware update/fix) Notify clinical staff of the issue as well as the updated skin temperature accuracy for the Affected Product - (For customers who do not wish to receive remote firmware update/fix) Please stop use of the Affected Devices and return them to BioIntelliSense, where possible. Notify or make aware all clinical staff of the recall issues and notify any additional facilities where the Affected Devices may have been further transferred. For questions or assistance - contact BioIntelliSense Customer Support at 888.908.8804 or email address - [email protected]

Distribution

U.S.: CA, CO, MA, TN, and TX O.U.S.: not provided

Quantity

135,414 devices (U.S. 95,414 and O.U.S. 40,000)