Device recall
Z-1013-2012: CI healthcare***Model: CI8092***S/N: 5-60-85-044 MFD: JUN, 2010 MADE IN…
FDA device recall · Class II · Cardiopulmonary Instrumentation, Inc
Key facts
| Recall number (Z-number) | Z-1013-2012 |
|---|---|
| Recall event | 59094 |
| Product | CI healthcare***Model: CI8092***S/N: 5-60-85-044 MFD: JUN, 2010 MADE IN CHINA***cihealthcare.com This stainless steel stretcher is used for transporting patients. |
| Product code | FPO |
| Recalling firm | Cardiopulmonary Instrumentation, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 19, 2012 |
| FEI number | 1034275 |
At a glance
- None 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