CAIRE Liberator 30 — Class I medical device recall Z-0338-2023
Terminated recall by Caire, Inc., reported 2022-12-14, distributed nationwide. An audit discovered some inconsistencies in weld penetration on the longitudinal weld seam on the inner bottle
| Recall number | Z-0338-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Caire, Inc., Ball Ground, GA, United States |
| Recall initiated | 2022-10-10 |
| Classified | 2022-12-02 |
| Reported by FDA | 2022-12-14 |
| Terminated | 2024-08-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CL, CO, DE |
| Quantity | 5 devices |
| Serial numbers | CBB3022300368, CBB3022300390, CBB3022300470, CBB3022300472, CBB3022300479 |
| Model numbers | 13337403 |
Product
CAIRE Liberator 30, MODEL 13337403, 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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0338-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.