Braemar Manufacturing recalls

Braemar Manufacturing has 3 recalls on record with the FDA and USDA, the earliest in 2020 and the latest reported on 1 Jan 2025. 1 is still ongoing. The most frequent reason is device malfunction.

Total recalls3since 2020

Last 12 months0reported

Class I133% of total

Ongoing1latest 1 Jan 2025

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 1Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 1 33%Class II 2 67%Class III 0 0%

Why braemar manufacturing is recalled

Device Malfunction3100%

Product types

Patient Monitors3100%

By year

2025133%
2020267%

Ongoing braemar manufacturing recalls

1 active

Reported	Class	Recall	Company	Reason	Where
1 Jan 2025Device	CLASS I	Monitoring Service Application (MSA) recalled by Braemar Manufacturing	Braemar Manufacturing	Device Malfunction	Nationwide

All braemar manufacturing recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
1 Jan 2025Device	CLASS I	Monitoring Service Application (MSA) recalled by Braemar Manufacturing	Braemar Manufacturing	Device Malfunction	Nationwide
18 Mar 2020Device	CLASS II	DL900 Holter Monitor 1285 Corporate Center Dr recalled	Braemar Manufacturing	Device Malfunction	Nationwide
18 Mar 2020Device	CLASS II	DL950 Holter Monitor 1285 Corporate Center Dr recalled	Braemar Manufacturing	Device Malfunction	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.