Beevers Manufacturing & Supply recalls

Beevers Manufacturing & Supply has 3 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 10 Dec 2014. The most frequent reason is sterility.

Total recalls3since 2014

Last 12 months0reported

Class I00% of total

Ongoing0latest 10 Dec 2014

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 3 100%Class III 0 0%

Why beevers manufacturing & supply is recalled

Sterility267%
Other Reasons133%

Product types

Heart & Vascular Devices267%
Other Medical Devices133%

By year

20143100%

All beevers manufacturing & supply recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
10 Dec 2014Device	CLASS II	Cannulaide, Model 101. The Cannulaide product is composed of die-cut recalled	Beevers Manufacturing & Supply	Sterility	Nationwide
3 Dec 2014Device	CLASS II	Cannulaide, Model 101, 102, 103. Respirator. The Cannulaide product recalled	Beevers Manufacturing & Supply	Sterility	7 states
20 Aug 2014Device	CLASS II	Luma Wrap Phototherapy Swaddler is designed to provide recalled	Beevers Manufacturing & Supply	Other	OR

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.