Braemar Manufacturing recalls MSA software versions 6.5-7.4 due to potential ECG events not being properly analyzed. Affected users should contact for updates.
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.
Braemar Manufacturing recalls software versions 6.5 to 7.4 that processes heart rhythm data. The software may not correctly analyze some heart rhythm events received between July 2022 and July 2024, which could lead to missed health issues.
The software has a disabled analysis step that may cause some heart rhythm events to be missed during review. This could lead to undetected health issues if the software fails to properly analyze critical cardiac events.
Users of Braemar's Monitoring Service Application software versions 6.5 to 7.4 who process heart rhythm data. People with cardiac monitoring devices connected to this software are most at risk.
Check if you have Braemar Monitoring Service Application software versions 6.5 through 7.4. The software processes heart rhythm data from connected medical devices.
Identify your software version by checking the product description or documentation.
The software may not properly analyze some heart rhythm events received between July 2022 and July 2024 due to a disabled analysis step.
The recall record does not specify a remedy, so contact Braemar Manufacturing for guidance.
The recall record does not mention a risk of serious injury, so the danger level is low risk.
We’ve drafted a message you can send Braem: Monitoring Service Application to request your refund or repair — edit it as you like.
Subject: Recall Z-0708-2025 — Braem: Monitoring Service Application Braem: Monitoring Service Application Hello, I own a Braem: Monitoring Service Application that is covered by recall Z-0708-2025 from Braem: Monitoring Service Application. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
