Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0339-2023 — CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit

U.S. FDA — Device Enforcement · United States · 2022-10-10 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0339-2023
Date of alert
2022-10-10
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Caire, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
13256195
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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