Feather-Flex Non-Conductive Adult Anesthesia Circuit (2021-04-16)

Starting date:

April 16, 2021

Posting date:

April 29, 2021

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-75495

Last updated:
2021-04-29

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  Reason
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  Affected products

Affected Products 

Feather-Flex Non-Conductive Adult Anesthesia Circuit

Reason

On April 15, 2021, it was discovered internally at BOMImed that during the manufacturing process, a very small number of corrugated tubes were damaged leading to a leaking tube. Out of caution, BOMImed is notifying customers and providing replacement circuits from the affected batch.

Affected products