FDA recall record

CAIRE Liberator 30, MODEL 13337403, Liquid Oxygen System Unit recall — FDA Z-0338-2023

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.

Class Iclassification
Z-0338-2023official record ID
Dec 14, 2022report date

Recall record at a glance

Official recordZ-0338-2023
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmCaire, Inc.
Report dateDec 14, 2022
Recall initiation dateOct 10, 2022
Quantity5 devices
LocationBall Ground, GA, United States

Official product description

CAIRE Liberator 30, MODEL 13337403, Liquid Oxygen System Unit

Why the product was 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.

Distribution information

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

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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