Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
CAIRE Liberator 20 Recalled by Caire, Inc. Due to An audit discovered some inconsistencies in weld penetration...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Caire, Inc. directly.
Affected Products
CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit
Quantity: 3 units
Why Was This 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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Caire, Inc.
Caire, Inc. has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report