Caire, Inc.: Medical Device Recall in 2022 - (Recall #: Z-0339-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit

Product Classification:

Class I

Date Initiated: October 10, 2022

Date Posted: December 14, 2022

Recall Number: Z-0339-2023

Event ID: 90999

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.

Status: Terminated

Product Quantity: 3 units

Code Information:

UDI/DI M766133374030M766132561950, Serial Numbers: CBB3022320073, CBB3022320077, CBB3022320074

Distribution Pattern:

US Nationwide - Worldwide Distribution: CA, NC, OH, AZ, and Canada, Chile, Colombia, and Germany

Voluntary or Mandated:

Voluntary: Firm initiated