Giraffe OmniBed (2018-10-11)

Starting date:

October 11, 2018

Posting date:

November 28, 2018

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-68378

• Reason
• Affected products

Affected products

Giraffe OmniBed

Reason

GE Healthcare has become aware of a potential safety issue that can occur if the canopy seals are not cleared appropriately per giraffe omnibed cleaning and care guidelines on systems with original seal design. Reported buildup of debris around the edge of the canopy seal can lead to a source of infection.

Affected products