Ohmeda Medical, A division of Datex-Ohmeda, Inc. Ohmeda Medical''s Giraffe OmniBeds and Giraffe Incubators Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Ohmeda Medical''s Giraffe OmniBeds and Giraffe Incubators
Brand
Ohmeda Medical, A division of Datex-Ohmeda, Inc.
Lot Codes / Batch Numbers
Serial Numbers: HDHE50001 to HDHE50164, HDHF50001 to HDHF50357, HDHF52001 to HDHF52212, HDHF53001 to HDHF53156, HDHF54001 to HDHF54168, HDHG54001 to HDHG54320, HDGD50200 to HDGD50389, HDGE50001 to HDGE50591, HDGF50001 to HDGF50046, HDGF52001 to HDGF52036, HDGF53001 to HDGF53102, HDGF54001 to HDGF54190, HDGG54001 to HDGG54367
Products Sold
Serial Numbers: HDHE50001 to HDHE50164; HDHF50001 to HDHF50357; HDHF52001 to HDHF52212; HDHF53001 to HDHF53156; HDHF54001 to HDHF54168; HDHG54001 to HDHG54320; HDGD50200 to HDGD50389; HDGE50001 to HDGE50591; HDGF50001 to HDGF50046; HDGF52001 to HDGF52036; HDGF53001 to HDGF53102; HDGF54001 to HDGF54190; HDGG54001 to HDGG54367
Ohmeda Medical, A division of Datex-Ohmeda, Inc. is recalling Ohmeda Medical''s Giraffe OmniBeds and Giraffe Incubators due to Neonatal incubators and beds may unintentionally move from a safe position following an interruption in the power supply.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Neonatal incubators and beds may unintentionally move from a safe position following an interruption in the power supply.
Recommended Action
Per FDA guidance
Ohmeda Medical notified consignees 04/25/05 by letter flagged as an 'Urgent Medical Device Correction'. The serial number specific notification advised that the elevating base may move following the mains power interruption. The letter further advised that the notice should not be confused with a previous (medical device correction) letter sent concerning movement of the elevating base caused by the footswitches on the device. Ohmeda indicated in the letter that users may continue to use the device with stated precautions, pending hardware upgrade by the firm''s service technologists.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026