Device recall
Z-0339-2023: CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit
FDA device recall · Class I · Caire, Inc.
Key facts
| Recall number (Z-number) | Z-0339-2023 |
|---|---|
| Recall event | 90999 |
| Product | CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit |
| Product code | BYJ |
| Recalling firm | Caire, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 19, 2024 |
| 510(k) numbers | K800742 |
| FEI number | 3004972304 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database