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BioButton Rechargeable Device, Multi-Patient

BIOINTELLISENSE, INC. · Model BBRM-B-I-N · UDI-DI 00850005949442

DRGDRT Prescription
1
510(k) clearances
1,732
Adverse events (73 deaths)
12
Recalls
125
Facilities

Description

The BioButton System (Multi-patient) is a remote monitoring wearable device intended for continuous collection of physiological data in home and healthcare settings while the patient is at rest. This could include heart rate, respiratory rate, skin temperature, and other data such as activity level, body position, sleep, and step and gait analysis. Data are securely transmitted via wireless connection for storage, review, analysis, and display. The Device can include the ability to display data and notify healthcare professionals when physiological data fall outside clinician-specified parameters. The data from the Device are intended as an aid to diagnosis, disease management, and treatment. The Device is intended for use on patients who are 18 years of age or older. The Device is not intended to output physiological measurements while the patient undergoes significant motion or is active. The Device is not intended for critical care. This Device is cleared in K241101 to be reprocessed and reused.

Recalls

DateFirmReason
2026-07-20Midmark CorporationA communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.
2024-07-19Biointellisense Inc.Software anomaly causing the skin temperature measurement accuracy to be slightly out of specification.
2021-01-08Nihon Kohden America IncIncorrect Date Stamp or No Data Transfer on Telemetry Receiver and Transmitter.
2020-05-21Vitalconnect Inc.A healthcare provider (HCP) noticed a patient had a lowered historic SpO2 reading that the software should have triggered a notification to the care team, but no notification was f
2017-05-15Boston Scientific CorporationThe device history record (DHR) was missing its test documentation for final HIPOT (high potential) electrical testing.
2017-03-02Philips VisicueCareCoordinator (eCC) is intended for use in data aggregation, patient interaction facilitation, storage and clinical information management with independent physiological device
2016-03-10Philips VisicuThe adherence check generates a software error. Two issues occur as a result of the software error: 1) No adherence flag is generated for that day; 2) No task is generated for the
2012-02-24BRAEMAR, INC.Braemar has recently became aware of a battery related incident that occurred with EWT battery packs that are used in a Braemer ER920W wireless event monitor and Fusion device. Th
2011-05-02BRAEMAR, INC.Braemar Inc., became aware of a battery related incident that occurred with an Able battery pack being used in a Braemar ER920W wireless event monitor. The event did not result i
2007-12-13Lifesync CorporationLifeSync Wireless ECG System - Intermittent failure when using LS-202 and LS-232 LeadWear in conjunction with LS-41245 and LS-41285 Adaptors. The out of box failure manifests as a

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.