Device recall
Z-0935-2007: HUMIDIFLOW Respiratory Gas Humidifier; Manufactured by: Porous Media Corporation…
FDA device recall · Class II · Porous Media Corporation
Key facts
| Recall number (Z-number) | Z-0935-2007 |
|---|---|
| Recall event | 37863 |
| Product | HUMIDIFLOW Respiratory Gas Humidifier; Manufactured by: Porous Media Corporation 1350 Hammond Road St Paul, MN 55110, Part Number HMK-RM |
| Product code | BTT |
| Recalling firm | Porous Media Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 10, 2011 |
| 510(k) numbers | K062091 |
| FEI number | 1000221012 |
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