Every recall we track for Braemar Manufacturing, LLC — 3 in all — plus the complaints and injury reports the public filed about them.
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.
Braemar recalls DL900 Holter Monitors made before Jan 1, 2020 that display Error 602 when starting new patient studies. The device may not function properly but stored ECG data can still be downloaded.
Braemar recalls DL950 Holter Monitors made before January 1, 2020 that may display Error 602 and fail to start new patient studies with AAA batteries.
