FDA Device recall Z-0336-2023
CAIRE Liberator 45, MODEL 13261699, Liquid Oxygen System Unit
- FDA Device
- Class I
- terminated
- Published 2022-12-14
On 2022-12-14 the FDA classified a Class I recall of CAIRE Liberator 45, MODEL 13261699, Liquid Oxygen System Unit by Caire, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0336-2023 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2022-10-10 |
| Published | 2022-12-14 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Caire |
| Distribution | US |
Product
CAIRE Liberator 45, MODEL 13261699, Liquid Oxygen System Unit
Reason
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.
Identifiers
| code_info | UDI/DI M766132616990, Serial Numbers: CBB3022310887, CBB3022310888, CBB3022310852, CBB3022310823, CBB3022310792, CBB30…UDI/DI M766132616990, Serial Numbers: CBB3022310887, CBB3022310888, CBB3022310852, CBB3022310823, CBB3022310792, CBB3022310843, CBB3022310844, CBB3022310827, CBB3022310842, CBB3022310845 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0336-2023%22
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