Ohmeda Medical recalls

Ohmeda Medical has 13 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 16 Oct 2019. The most frequent reason is temperature abuse.

Total recalls13since 2017

Last 12 months0reported

Class I00% of total

Ongoing0latest 16 Oct 2019

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 13 100%Class III 0 0%

Why ohmeda medical is recalled

Product types

By year

201918%
201818%
20171185%

All ohmeda medical recalls, newest first

13 total

Reported	Class	Recall	Company	Reason	Where
16 Oct 2019Device	CLASS II	Giraffe Omnibed recalled by Ohmeda Medical	Ohmeda Medical	Lead & Heavy Metals	Nationwide
4 Apr 2018Device	CLASS II	Rotating IV Pole Rotating IV Pole falls under the category recalled	Ohmeda Medical	Other	Nationwide
29 Mar 2017Device	CLASS II	Giraffe Exam Light The Exam Light illuminates body surfaces recalled	Ohmeda Medical	Other	Nationwide
29 Mar 2017Device	CLASS II	Giraffe OmniBed Ohmeda Medical Omnibed- The OmniBed is recalled	Ohmeda Medical	Temperature Abuse	Nationwide
29 Mar 2017Device	CLASS II	IWS Infant Warmer System-Infant radiant warmers provide recalled	Ohmeda Medical	Temperature Abuse	Nationwide
29 Mar 2017Device	CLASS II	Giraffe Incubator The Giraffe Incubator is an infant incubator recalled	Ohmeda Medical	Temperature Abuse	Nationwide
29 Mar 2017Device	CLASS II	Giraffe Spot PT Ohmeda Medical Spot PT Lite Phototherapy recalled	Ohmeda Medical	Other	Nationwide
29 Mar 2017Device	CLASS II	Giraffe OmniBed Ohmeda Medical Giraffe OmniBed- The OmniBed recalled	Ohmeda Medical	Temperature Abuse	Nationwide
29 Mar 2017Device	CLASS II	Giraffe Bedded Warmer, Panda Warmer Modifiction to Giraffe recalled	Ohmeda Medical	Device Malfunction	Nationwide
29 Mar 2017Device	CLASS II	Giraffe Bedded Warmer, Panda Warmer Modification to Giraffe recalled	Ohmeda Medical	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.