FDAOctober 5, 2018device

Giraffe Omnibed - Product Usage: The OmniBed is a combination of an infant incubator and an infant warmer. The device can be operated as an incubator or as a warmer and can transition from one mode to the other on user s demand. It cannot be operated in both modes at the same time. Incubators and...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

GE Healthcare has become aware of a potential safety issue that can occur if the canopy seals are not cleaned appropriately. Healthcare professionals reported buildup of debris around the edge of the canopy seal which can lead to a source of infection. Upon review, the Agency concluded that the cleaning and care guidelines provided by the firm were inadequate for effective cleaning of the device. In particular, the instructions do not instruct for removal of canopy seal prior to cleaning, which leads to the buildup of debris.

What to do

FDA enforcement status: Terminated

Brands named

ohmeda medicalohmeda

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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