Health product recall

Liberator Stationary Liquid Oxygen Device

Brand(s)
Last updated

Summary

Product
Liberator Stationary Liquid Oxygen Device
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information.

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

Liberator Stationary Liquid Oxygen Device

CBB3022320074
CBB3022310852
CBB3022310843
CBB3022310827
CBB3022310823
CBB3022310842
CBB3022310845
CBB3022320077
CBB3022310792
CBB3022310844

13261699
13256195

Issue

There were inconsistencies in weld penetration on the longitudinal weld seam on the inner bottle. This can lead to premature inner vessel failure. The failure mode would be potential loss of vacuum, which could cause either an over-delivery of oxygen or the outer vessel to frost. Increased flow of oxygen from the relief valves could lead to an increased fire risk.

Recall start date: October 11, 2022

Additional information

Details
Original published date: 2022-11-09
Alert / recall type
Health product recall
Category
Health product - Medical device - Anaesthesiology
Companies

Caire Inc.

2200 Airport Industrial Drive, Ball Ground, Georgia, United States, 30107

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-72172