Device recall
Z-0949-2013: TotalCare SpO2RT2 bed. Product Usage: Bed, flotation therapy, powered bed may be…
FDA device recall · Class II · Hill-Rom, Inc.
Key facts
| Recall number (Z-number) | Z-0949-2013 |
|---|---|
| Recall event | 64580 |
| Product | TotalCare SpO2RT2 bed. Product Usage: Bed, flotation therapy, powered bed may be used in a variety of settings including, but not limited to, acute care, including critical care, step down/progressive care, medical/surgical, high acuity sub-acute care, post anesthesia care unit (PACU), and sections… |
| Product code | IOQ |
| Recalling firm | Hill-Rom, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 16, 2014 |
| 510(k) numbers | K970636 |
| FEI number | 1824206 |
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