Device recall
Z-0396-2011: CIVCO Posifix Extension, REF MTIL6606, Reusable non-sterile extension for use…
FDA device recall · Class II · Med Tec Inc
Key facts
| Recall number (Z-number) | Z-0396-2011 |
|---|---|
| Recall event | 55999 |
| Product | CIVCO Posifix Extension, REF MTIL6606, Reusable non-sterile extension for use with the Universal Couchtop. The firm name on the label is CIVCO, Orange City, IA. For use to support and aid in positioning a patient during radiologic and other medical procedures. |
| Product code | IXQ |
| Recalling firm | Med Tec Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 17, 2012 |
| 510(k) numbers | K973842 |
| FEI number | 1000143606 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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