Device recall
Z-1423-2011: HomeFill Oxygen Compressor IOH200 Homefill, The serial numbers are as follows…
FDA device recall · Class II · Invacare Corporation
Key facts
| Recall number (Z-number) | Z-1423-2011 |
|---|---|
| Recall event | 57629 |
| Product | HomeFill Oxygen Compressor IOH200 Homefill, The serial numbers are as follows: 10JF034081, 10JF034082, 10JF034083, 10JF034084, 10JF034085, 10JF034086, 10JF034087, 10JF034088, 10JF034089, 10JF034090, 10JF034091, 10JF034092, 10JF034093, 10JF034094, 10JF034095, 10JF034096, 10JF034097, 10JF034098… |
| Product code | CAW |
| Recalling firm | Invacare Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 21, 2011 |
| 510(k) numbers | K003939 |
| FEI number | 3002889431 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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