Recall database

Braemar Manufacturing, LLC recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–1 of 1 recalls

Class IOngoingZ-0708-2025

Braemar Manufacturing, LLC recalls Monitoring Service Application (MSA). Software to process

Not all Electrocardiogram (ECG) events received July 2022-July 2024 were not properly routed and subsequently reviewed due to an analysis step being disabled with the monitoring service application software.

Electrocardiograph
Use error

Braemar Manufacturing,…CAJan 1, 2025