ADULT ANESTHESIA BREATHING CIRCUIT (2021-07-14)

Starting date:

July 14, 2021

Posting date:

July 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-76097

Last updated:
2021-07-30

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  Reason
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  Affected products

Affected Products 

ADULT ANESTHESIA BREATHING CIRCUIT

Reason

Westmed received several complaints pertaining to leaks and holes in the tubing. The issue of leakage was caused due to a sporadic drag along the pulley guide that caused perforations in the tubing.

Affected products