PlainRecalls
FDA Devices Critical Class I Terminated

CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit

Reported: December 14, 2022 Initiated: October 10, 2022 #Z-0339-2023

Product Description

CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit

Reason for Recall

An audit discovered some inconsistencies in weld penetration on the longitudinal weld seam on the inner bottle of the device on some of the units.

Details

Recalling Firm
Caire, Inc.
Units Affected
3 units
Distribution
US Nationwide - Worldwide Distribution: CA, NC, OH, AZ, and Canada, Chile, Colombia, and Germany
Location
Ball Ground, GA

Frequently Asked Questions

What product was recalled?
CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit. Recalled by Caire, Inc.. Units affected: 3 units.
Why was this product recalled?
An audit discovered some inconsistencies in weld penetration on the longitudinal weld seam on the inner bottle of the device on some of the units.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 14, 2022. Severity: Critical. Recall number: Z-0339-2023.