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Braemar recalls

Braemar has 2 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 10 Jul 2013. The most frequent reason is device malfunction.

Total recalls2since 2013

Last 12 months0reported

Class I00% of total

Ongoing0latest 10 Jul 2013

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '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 0 0%Class II 2 100%Class III 0 0%

Why braemar is recalled

Device Malfunction2100%

Product types

Other Medical Devices2100%

By year

20132100%

All braemar recalls, newest first

2 total

Reported	Class	Recall	Company	Reason	Where
10 Jul 2013Device	CLASS II	Lithium Thionyl non-rechargeable disposable battery pack recalled	Braemar	Device Malfunction	Nationwide
10 Jul 2013Device	CLASS II	Lithium Thionyl non-rechargeable disposable battery pack recalled	Braemar	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.