Device recall
Z-1298-03: Integris Monitor Arm, model P997-01.
FDA device recall · Class II · Hill-Rom Co., Inc.
Key facts
| Recall number (Z-number) | Z-1298-03 |
|---|---|
| Recall event | 26933 |
| Product | Integris Monitor Arm, model P997-01. |
| Product code | MHX |
| Recalling firm | Hill-Rom Co., Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 19, 2004 |
| FEI number | 1824206 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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